{"id":16,"date":"2016-10-27T16:03:59","date_gmt":"2016-10-27T07:03:59","guid":{"rendered":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/ohmorilab\/wordpress\/?page_id=16"},"modified":"2026-04-25T17:33:22","modified_gmt":"2026-04-25T08:33:22","slug":"%e7%99%ba%e8%a1%a8%e8%ab%96%e6%96%87","status":"publish","type":"page","link":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=16","title":{"rendered":"\u767a\u8868\u8ad6\u6587"},"content":{"rendered":"<ul id=\"cnav\">\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=16\/#2021-2025\">2021\u5e74\u4ee5\u964d<\/a><\/li>\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=16\/#2016-2020\">2016-2020\u5e74<\/a><\/li>\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=16\/#2011-2015\">2011-2015\u5e74<\/a><\/li>\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=16\/#2006-2010\">2006-2010\u5e74<\/a><\/li>\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=16\/#2001-2005\">2001-2005\u5e74<\/a><\/li>\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=66\/#1996-2000\">1996-2000\u5e74<\/a><\/li>\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=66\/#1991-1995\">1991-1995\u5e74<\/a><\/li>\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=66\/#1986-1990\">1986-1990\u5e74<\/a><\/li>\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=66\/#1978-1985\">1978-1985\u5e74<\/a><\/li>\n<li><a href=\"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=52\">\u8457 \u66f8<\/a><\/li>\n<\/ul>\n<h2 id=\"2021-2025\">2021\u5e74\u4ee5\u964d<\/h2>\n<table class=\"color\">\n<tbody>\n<tr>\n<td>306.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/ceur.70269\">Site-Selective Oxidative Dimerization of Oxaphenalenone Scaffolds: Total Synthesis of (\u00b1)-Bacillosporin C<\/a>, <em>ChemistryEurope<\/em>, <strong>4<\/strong>, e70269 (2026), by Y. Qian, T. Sugai, T. Saitoh, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>305.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/aces.onlinelibrary.wiley.com\/doi\/full\/10.1002\/asia.202500921\">Fluorinated <em>Para<\/em>-Quinone Monoacetal: Versatile Reactivity for Constructing Functionalized Scaffolds<\/a>, <em>Chem. Asian J.<\/em>, <strong>11<\/strong>, e00921 (2025), by K. Azami, M. Morita, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>304.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/academic.oup.com\/chemlett\/article\/54\/11\/upaf186\/8281821\">Synthetic study on \u03b3-rubromycin: spiroacetal formation by using photochemical reaction of 2-hydroxy-1,4-naphthoquinone<\/a>, <em>Chem. Lett.<\/em>, <strong>11<\/strong>, upaf186 (2025), by Y. Ando, D. Ogawa, S. Morishita, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>303.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/ceur.202500086\">Synthetic Study on Bicyclic Pyranonaphthoquinone Natural Products: Construction of the Dioxabicyclo[3.3.1]nonene Motif<\/a>, <em>ChemistryEurope<\/em>, <strong>3<\/strong>, e202500086(2025), by Y. Ando, S. Ajima, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>302.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202415108\">Total Syntheses of \u03b2- and \u03b3-Naphthocyclinones<\/a>, <em>Angew. Chem. Int. Ed.<\/em>, <strong>64<\/strong>, e202415108 (2024), by Y. Ando, T. Hoshino, N. Tanaka, M. M. Maturi, Y. Nakazawa, T. Fukazawa, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>301.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403924004118\">Facile synthetic route to isoxazoles from \u03b2-sulfinyl- and \u03b2-sulfonyl-cyclohexenones via regioselective nitrile oxide cycloaddition and in-situ elimination<\/a>, <em>Tetrahedron. Lett.<\/em>, <strong>151<\/strong>, 155316 (2024), by K. Murata, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>300.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.4c01530\" target=\"_blank\" rel=\"no noopener opener noreferrer\">One-Pot Synthesis of Functionalized Benzotropones via a Phthalide Ring-Opening\/Intramolecular Aldol Condensation Cascade<\/a>, <em>Org. Lett.<\/em>, <strong>26<\/strong>, 5120 (2024), by S. Yeom, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>299.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.3c03791\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Total Syntheses of Sparsomycin and Sparoxomycins A<sub>1<\/sub> and A<sub>2<\/sub> via Sulfenate-Anion-Mediated Iterative C\u2013S Bond Formation<\/a>, <em>Org. Lett.<\/em>, <strong>25<\/strong>, 9036 (2023), by J. Zhang, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>298.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2196-5592\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Diastereoselective Access to <em>anti<\/em>-\u03b2-Hydroxy Sulfoxides from \u00adChiral Epoxides and Prochiral Sulfenate Anions: Mechanistic \u00adInsights, Scope, and Limitation<\/a>, <em>Synlett<\/em>, <strong>35<\/strong>, 1458 (2023), by J. Zhang, V. -V. Betkekar, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>297.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/abstract\/10.1055\/a-2124-4161\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Study on Integrated Synthesis of Dimeric Pyranonaphthoquinones: Preparation of Versatile Synthetic Intermediate and Conversion into <em>ent<\/em>-Hemi-actinorhodin and <em>ent<\/em>-Hemi-\u03b3-actinorhodin<\/a>, <em>Synlett<\/em>, <strong>34<\/strong>, 2011 (2023), by Y. Ando, M. -M. Matsuri, T. Hoshino, N. Tanaka, T. Sakai, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>296.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2113-0212\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Photochemical Reaction of 1,2-Naphthoquinone toward Enantioselective Synthesis of \u03b3-Rubromycin: Viability Dependence on Chromophore<\/a>, <em>Synlett<\/em>, <strong>35<\/strong>, 441 (2023), by Y. Ando, D. Ogawa, F. Wakita, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>295.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402023002399?dgcid=author\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Stereospecific naphthoquinone photoredox reactions: Total syntheses of spirocyclic natural products<\/a>, <em>Tetrahedron<\/em>, <strong>139<\/strong>, 133448 (2023), by Y. Ando, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>294.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202213682\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Enantioselective Total Syntheses of Preussomerins: Control of Spiroacetal Stereogenicity by Photochemical Reaction of a Naphthoquinone through 1,6-Hydrogen Atom Transfer<\/a>, <em>Angew. Chem. Int. Ed.<\/em>, <strong>62<\/strong>, e202213682 (2023), by Y. Ando, D. Ogawa, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>293.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2022\/ob\/d2ob01416e\" target=\"_blank\" rel=\"no noopener opener noreferrer\"><em>De novo<\/em> synthesis of dimerization-ready flavan unit <em>via<\/em> intramolecular Pummerer\/Friedel\u2013Crafts cascade<\/a>, <em>Org. Biomol. Chem.<\/em>, <strong>20<\/strong>, 7419  (2022), by V. -V. Betkekar, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>292.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202205106\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Total Synthesis of Parameritannin\u2005A2, a Branched Epicatechin Tetramer with Two Double Linkages<\/a>, <em>Angew. Chem. Int. Ed.<\/em>, <strong>61<\/strong>, e202205106 (2022), by V. -V. Betkekar, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>291.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.1c04306\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Total Synthesis and Structure Assignment of Saptomycin H<\/a>, <em>Org. Lett.<\/em>, <strong>24<\/strong>, 1439 (2022), by J. Shimura, Y. Ando, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>290.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/abstract\/10.1055\/s-0040-1719840\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Group-Selective Approaches to Complex Natural Product Synthesis: Three Examples of Diastereotopos-Selective Reactions<\/a>, <em>Synlett<\/em>, <strong>33<\/strong>, 429 (2021), by K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>289.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0040-1719836\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Synthetic Study on Carthamin, Part 4. Improved Synthesis of a <em>C<\/em>-Glycosyl Quinochalcone by Installation of a Side Chain through Regioselective De-<em>O<\/em>-methylation and Acyl Rearrangement<\/a>, <em>Synlett<\/em>, <strong>32<\/strong>, 2046-2052 (2021), by S. Matsuoka, K. Azami, Y. Fujiki, R. Dohi, T. Yasuike, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>288.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.journal.csj.jp\/doi\/full\/10.1246\/bcsj.20210053\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Model Study toward Total Synthesis of Dimeric Pyranonaphthoquinones: Synthesis of Hemi-Actinorhodin<\/a>, <em>Bull. Chem. Soc. Jpn.<\/em>, <strong>94<\/strong>, 1364-1376 (2021), by Y. Ando, T. Fukazawa, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>287.<\/td>\n<td><a class=\"blank\" href=\" https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/hlca.202100008\" rel=\"no noopener opener noreferrer\">Photoredox Reaction of Naphthoquinone <em>C<\/em>\u2010Glycoside Revisited: Insight into Stereochemical Aspect<\/a>, <em>Helv. Chim. Acta<\/em>, <strong>104<\/strong>, e2100008 (2021), by Y. Ando, T. Matsumoto, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>286.<\/td>\n<td><a class=\"blank\" href=\" https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-1303-5613\" rel=\"no noopener opener noreferrer\">Synthetic Study on Acremoxanthone A, Part 2: Model Study on the EFG Xanthone Moiety through a Nitrile Oxide Cycloaddition\u2013S<sub>N<\/sub>Ar Sequence<\/a>, <em>Synlett<\/em>, <strong>32<\/strong>, 423-428 (2021), by H. Nakakohara, Y. Hirano, K. Ohmori, H. Takikawa, K. Suzuki<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2 id=\"2016-2020\">2016-2020\u5e74<\/h2>\n<table class=\"color\">\n<tbody>\n<tr>\n<td>285.<\/td>\n<td><a class=\"blank\" href=\" https:\/\/www.journal.csj.jp\/doi\/abs\/10.1246\/cl.200411\" rel=\"no noopener opener noreferrer\">Thiolate-mediated Reductive Cyclizations: Scope, Limitation and Novel Mechanistic Insights<\/a>, <em>Chem. Lett.<\/em>, <strong>49<\/strong>, 1103-1106 (2020), by Y. Ando, T. Fukazawa, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>284.<\/td>\n<td><a class=\"blank\" href=\" https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0040-1707198\" rel=\"no noopener opener noreferrer\">Synthetic Study on Lactonamycins, Part 2: Stereoselective Access to ABCD-Ring System<\/a>, <em>Synlett<\/em>, <strong>31<\/strong>, 1623-1628 (2020), by H. Takikawa, K. Murata, S. Sato, T. Kawada, H. Nakakohara, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>283.<\/td>\n<td><a class=\"blank\" href=\" https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.202003131\" rel=\"no noopener opener noreferrer\">Intramolecular Benzyne\u2013Phenolate [4+2] Cycloadditions<\/a>, <em>Angew. Chem. Int. Ed.<\/em>, <strong>59<\/strong>, 12440-12444 (2020), by H. Takikawa, A. Nishii, H. Takiguchi, H. Yagishita, M. Tanaka, K. Hirano, M. Uchiyama, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>282.<\/td>\n<td><a class=\"blank\" href=\" https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c00354\" rel=\"no noopener opener noreferrer\">Synthesis of Enantiopure <em>C2<\/em>-Symmetric Anthracenophane and Dimerization En Route to Multiple-Bridged Cyclophanes<\/a>, <em>Org. Lett.<\/em>, <strong>22<\/strong>, 2002-2006 (2020), by Y. Ueda, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>281.<\/td>\n<td><a class=\"blank\" href=\" https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.201901807\" rel=\"no noopener opener noreferrer\">Toward Pluramycins with Epoxy Side Chain: Syntheses of Kidamycinone and Epoxykidamycinone (Saptomycinone H)<\/a>, <em>Chem. Asian J.<\/em>, <strong>15<\/strong>, 828-832 (2020), by Y. Ando, Y. Maezawa, J. Shimura, K. Kitamura, T. Matsumoto, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>280.<\/td>\n<td><a class=\"blank\" href=\" https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b04127\" rel=\"no noopener opener noreferrer\">Hydroxylamine-Mediated Anthrapyranone Formation, Solving 5-<em>exo<\/em>\/6-<em>endo<\/em> Issue toward Synthesis of Pluramycin-Class Antibiotics<\/a>, <em>Org. Lett.<\/em>, <strong>22<\/strong>, 175-179 (2020), by J. Shimura, Y. Ando, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>279.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2019\/OB\/C9OB01896D#!divAbstract\" rel=\"no noopener opener noreferrer\">Syntheses of doubly linked proanthocyanidins using free flavan units as nucleophiles: insight into the origin of the high regioselectivity of annulation<\/a>, <em>Org. Biomol. Chem.<\/em>, <strong>17<\/strong>, 9129-9134 (2019), by V. -V. Betkekar, M. Harachi, K. Suzuki, K. Ohmori<\/td>\n<\/tr>\n<tr>\n<td>278.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.heterocycles.jp\/newlibrary\/libraries\/journal\/101\/2\/current\" target=\"_blank\" rel=\"no noopener opener noreferrer\">\u03b1-L-Vancosamine Aryl <em>C<\/em>-Glycosides, Less Stable Anomers: A Problem in Synthesis of Pluramycin-Class Antibiotics<\/a>, <em>Heterocycles<\/em>, <strong>101<\/strong>, 645-663 (2020), by Y. Ando, H. Asahina, K. Kitamura, T. Matsumoto, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>277.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201906762\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Stereochemical Dichotomy in Two Competing Cascade Processes: Total Syntheses of Both Enantiomers of Spiroxin A<\/a>, <em>Angew. Chem. Int. Ed.<\/em>, <strong>58<\/strong>, 12507-12513 (2019), by Y. Ando, D. Tanaka, R. Sasaki, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>276.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/doi.org\/10.1002\/anie.201900454\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Total Synthesis of Carthamin, a Traditional Natural Red Pigment<\/a>, <em>Angew. Chem. Int. Ed.<\/em>, <strong>58<\/strong>, 5321-5326 (2019), by K. Azami, T. Hayashi, T. Kusumi, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>275.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/epdf\/10.1002\/anie.201814172\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Total Synthesis of Actinorhodin<\/a>, <em>Angew. Chem. Int. Ed.<\/em>, <strong>58<\/strong>, 4264-4270 (2019), by M. Ninomiya, Y. Ando, F. Kudo, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>274.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/doi.org\/10.1055\/s-0037-1611654\" target=\"_blank\" rel=\"no noopener opener noreferrer\">General Synthetic Approach to Rotenoids via Stereospecific, Group-Selective 1,2-Rearrangement and Dual S<sub>N<\/sub>Ar Cyclizations of Aryl Fluorides<\/a>, <em>Synthesis<\/em>, <strong>51<\/strong>, 1139-1156 (2019), by S. Matsuoka, K. Nakamura, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>273.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/doi.org\/10.1039\/c8sc05518a\" target=\"_blank\" rel=\"no noopener opener noreferrer\">2-Bromo-6-(chlorodiisopropylsilyl)phenyl tosylate as an efficient platform for intramolecular benzyne-diene [4+2] cycloaddition<\/a>, <em>Chem. Sci.<\/em>, <strong>10<\/strong>, 3840-3845 (2019), by A. Nishii, H. Takikawa, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>272.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.ingentaconnect.com\/content\/scs\/chimia\/2018\/00000072\/00000012\/art00007;jsessionid=vcrob9d9eo6y.x-ic-live-03\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Synthesis of Oxygenated ortho-Methylbenzaldehydes via Aryne [2+2] Cycloaddition and Benzocyclobutenol Ring Opening<\/a>, CHIMIA <strong>2018<\/strong>, <em>72<\/em>, No. 12, 870-873, by M. -M. Maturi, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>271.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/doi.org\/10.1039\/C8CS00350E\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Aryne-based strategy in the total synthesis of naturally occurring polycyclic compounds<\/a>, <em>Chem. Soc. Rev<\/em>., <strong>47<\/strong>, 8030-8056 (2018), by H. Takikawa, A. Nishii, T. Sakai, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>270.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1002\/chem.201801064\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Photoredox Reactions of Quinones<\/a>, <em>Chem.<\/em> <em>Eur<\/em>. <em>J<\/em>., <strong>24<\/strong>, 15955-15964 (2018), by Y. Ando, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>269.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1021\/acs.orglett.8b01475\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Model Reactions for the Enantioselective Synthesis of \u03b3-Rubromycin: Stereospecific Intramolecular Photoredox Cyclization of an ortho-Quinone Ether to a Spiroacetal<\/a>, <em>Org. Lett.,<\/em> <strong>20<\/strong>, 3928-3932 (2018), by F. Wakita, Y. Ando, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>268.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1021\/acs.orglett.8b01366\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Total Syntheses of Pusilatins A\u2013C, Liverwort-Derived Macrocyclic Bisbibenzyl Dimers<\/a>, <em>Org.Lett.,&nbsp;<\/em><strong>20<\/strong>, 3579-3582 (2018), by T. Yamada, H. Takiguchi, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>267.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1016\/j.bmcl.2018.05.056\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Intramolecular photoredox reactions of 1,2-naphthoquinone derivatives<\/a>, <em>Bioorg. Med. Chem. Lett.<\/em>, <strong>28<\/strong>, 2663-2666 (2018), by Y. Ando, F. Wakita, K. Ohmori, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>266.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1055\/s-0037-1610136\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Total Synthesis of Bis-anthraquinone Antibiotic BE-43472B<\/a>, <em>Synthesis<\/em>, <strong>50<\/strong>, 2490-2515 (2018), by Y. Yamashita, Y. Hirano, A. Takada, H. Takikawa, K. Suzuki<\/td>\n<\/tr>\n<tr>\n<td>265.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1021\/acs.orglett.8b00873\" target=\"_blank\" rel=\"no noopener opener noreferrer\">Total Synthesis of Selligueain A, a Sweet Flavan Trimer<\/a>, <em>Org. Lett.,&nbsp;<\/em><strong>20<\/strong>, 2857\u20132861 (2018), by Y. Noguchi, R. Takeda, K. Suzuki and K. Ohmori.<\/td>\n<\/tr>\n<tr>\n<td>264.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1055\/s-0036-1591563\" target=\"_blank\" rel=\"no noopener opener noreferrer\">First Total Synthesis of Oxirapentyn D, a Highly Oxidized Chromene Natural Product<\/a>, <em>Synlett, <\/em><strong>29<\/strong>, 1351\u20131357 (2018),&nbsp;by T. Sakai, K. Ohmori and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>263.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1021\/acs.chemrev.7b00380\" target=\"_blank\" rel=\"noopener noreferrer\">Total Synthesis of Aryl <em>C<\/em>-Glycoside Natural Products: Strategies and Tactics<\/a>, <em>Chem. Rev.,&nbsp;<\/em><strong>118<\/strong>, 1495\u20131598 (2018), by K. Kitamura, Y. Ando, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>262.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1002\/anie.201707099\" target=\"_blank\" rel=\"noopener noreferrer\">First Total Syntheses of Tetracenomycins\u2005C and X<\/a>, <em>Angew. Chem. Int. Ed.,&nbsp;<\/em><strong>56<\/strong>, 12608\u201312613 (2017), by S. Sato, K. Sakata, Y. Hashimoto, H. Takikawa, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>261.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1002\/anie.201705562\" target=\"_blank\" rel=\"noopener noreferrer\">Stereospecificity in Intramolecular Photoredox Reactions of Naphthoquinones: Enantioselective Total Synthesis of (\u2212)-Spiroxin\u2005C<\/a>, <em>Angew. Chem. Int. Ed., <\/em><strong>56<\/strong>, 11460\u201311465 (2017), by Y. Ando, A. Hanaki, R. Sasaki, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>260.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1055\/s-0036-1590825\" target=\"_blank\" rel=\"noopener noreferrer\">Preparation of 2-Substituted 3-Methoxycarbonyl-4-methoxyfurans that Allow Access to Highly Functionalized Naphthalenes via Regioselective Cycloaddition with Alkoxybenzyne<\/a>, <em>Synlett,&nbsp;<\/em><strong>28<\/strong>, 1719-1723 (2017), by S. Sato, T. Kawada, H. Takikawa and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>259.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/doi.org\/10.1246\/cl.170328\" target=\"_blank\" rel=\"noopener noreferrer\">Oxidative Ring Opening of Benzocyclobutenone Oximes: Novel Access to Stable Nitrile Oxides<\/a>, <em>Chem. Lett.,&nbsp;<\/em><strong>46<\/strong>, 998\u20131000 (2017), by H. Takikawa, S. Sato, R. Seki, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>258.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0036-1589001\" target=\"_blank\" rel=\"noopener noreferrer\">Intramolecular Photoredox Reaction of Naphthoquinone Derivatives<\/a>, <em>Synlett, <\/em><strong>28<\/strong>, 1040-1045 (2017), by Y. Ando, T. Matsumoto and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>257.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.7b00464\" target=\"_blank\" rel=\"noopener noreferrer\">Enantioselective Access to Bicyclo[3.2.1]octadienone Skeleton: Total Syntheses of (+)-Engelharquinone and Its Epoxide<\/a>, <em>Org. Lett.,&nbsp;<\/em><strong>19<\/strong>, 1470\u20131473 (2017), by T. Fukazawa, Y. Ando, K. Ohmori, T. Hayashi and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>256.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0036-1588944\" target=\"_blank\" rel=\"noopener noreferrer\">Total Syntheses of Atrovenetin and Atrovenetinone: A Naphthalene-Annulation Approach to a Discoid Tricycle Using Allenic Acid<\/a>, <em>Synlett,&nbsp;<\/em><strong>28<\/strong>, 944-950 (2017), by K. Matsushita, K. Suzuki and K. Ohmori.<\/td>\n<\/tr>\n<tr>\n<td>255.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.6b03899\" target=\"_blank\" rel=\"noopener noreferrer\">Synthetic Study on Carthamin. 2. Stereoselective Approach to <i>C<\/i>-Glycosyl Quinochalcone via Desymmetrization<\/a>, <em>Org. Lett.,&nbsp;<\/em><strong>19<\/strong>, 866\u2013869 (2017), by T. Hayashi, K. Ohmori and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>254.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1002\/anie.201609253\" target=\"_blank\" rel=\"noopener noreferrer\">Stereocontrolled Total Syntheses of (\u2212)-Rotenone and (\u2212)-Dalpanol by 1,2-Rearrangement and S<sub>N<\/sub>Ar Oxycyclizations<\/a>, <em>Angew. Chem. Int. Ed.,&nbsp;<\/em><strong>56<\/strong>, 182\u2013187 (2017), by K. Nakamura, K. Ohmori and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>253.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0036-1588600\" target=\"_blank\" rel=\"noopener noreferrer\">Synthetic Study on Acremoxanthone A: Construction of Bicyclo[3.2.2]nonane CD Skeleton and Fusion of AB Rings<\/a>, <em>Synlett,&nbsp;<\/em><strong>28<\/strong>, 214\u2013220 (2017), by Y. Hirano, K. Tokudome, H. Takikawa and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>252.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1002\/hlca.201600244\" target=\"_blank\" rel=\"noopener noreferrer\">Total Synthesis of the Proposed Structure of Ardimerin, and Proposal for its Structural Revision<\/a>, <em>Helv. Chim. Acta,&nbsp;<\/em><strong>99<\/strong>, 944\u2013960 (2016), by R. Nakayama, E.-M. Tanzer, T. Kusumi K. Ohmori and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>251.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.6b02203\" target=\"_blank\" rel=\"noopener noreferrer\">Total Synthesis of (+)-Vicenin-2<\/a>, <em>Org. Lett.,&nbsp;<\/em><strong>18<\/strong>, 4488\u20134490 (2016), by T. C. Ho, H. Kamimura, K. Ohmori and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>250.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1246\/bcsj.20160134\" target=\"_blank\" rel=\"noopener noreferrer\">Pleospdione, A Tricyclic Natural Product with Dense Oxygenation at the A-Ring: Total Synthesis and Incongruity of the Originally Assigned Structure and its C3-Epimer<\/a>, <em>Bull. Chem. Soc. Jpn.,&nbsp;<\/em><strong>89<\/strong>, 941\u2013954 (2016), by H. Takikawa, Y. Ishikawa, Y. Toshinaga, Y. Hashimoto, T. Kusumi and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>249.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0035-1562514\" target=\"_blank\" rel=\"noopener noreferrer\">Synthesis of \u03b2-Hydroxynaphthoate Derivatives from Ketodioxinones via Benzyne Acyl-Alkylation and Aldol Condensation Cascade<\/a>, <em>Synthesis,&nbsp;<\/em><strong>48<\/strong>, 3331\u20133338 (2016), by H. Takikawa, A. Nishii and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>248.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0035-1562511\" target=\"_blank\" rel=\"noopener noreferrer\">Synthetic Study on Carthamin: Problem and Solution for Oxidative Dearomatization Approach to Quinol <i>C<\/i>-Glycoside<\/a>, <em>Synlett,&nbsp;<\/em><strong>27<\/strong>, 2345\u20132351 (2016), by T. Hayashi, K. Ohmori and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>247.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0035-1561654\" target=\"_blank\" rel=\"noopener noreferrer\">Facile Synthesis of Stereodefined \u03b1-Iodovinyl Sulfoxides, Versatile Platform to Trisubstituted Olefins<\/a>, <em>Synlett,&nbsp;<\/em><strong>27<\/strong>, 2024\u20132028 (2016), by S. Jung, Y. Ueda, K. Suzuki, and K. Ohmori.<\/td>\n<\/tr>\n<tr>\n<td>246.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0035-1561417\" target=\"_blank\" rel=\"noopener noreferrer\">First Total Synthesis of Dermocanarin 2<\/a>, <em>Synlett,&nbsp;<\/em><strong>27<\/strong>, 1262\u20131268 (2016), by S. Yamaguchi, N. Takahashi, D. Yuyama, K. Sakamoto, K. Suzuki and T. Matsumoto.<\/td>\n<\/tr>\n<tr>\n<td>245.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1055\/s-0035-1561937\" target=\"_blank\" rel=\"noopener noreferrer\">Stereocontrolled Synthesis of Planar Chiral Carba-Paracyclophanes via Modular Assembly<\/a>, <em>Synlett,&nbsp;<\/em><strong>27<\/strong>, 1521\u20131526 (2016), by S. Jung, Y. Kitajima, Y. Ueda, K. Suzuki, and K. Ohmori.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2 id=\"2011-2015\">2011-2015\u5e74<\/h2>\n<table class=\"color\">\n<tbody>\n<tr>\n<td>244.<\/td>\n<td style=\"text-align: left;\"><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.5b02906\" target=\"_blank\" rel=\"noopener noreferrer\">Total Syntheses of Perenniporides<\/a>, <em>Org. Lett.,&nbsp;<\/em><strong>17<\/strong>, 5634\u20135637 (2015), by M. Morita, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>243.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.5b01732\" target=\"_blank\" rel=\"noopener noreferrer\">Synthetic Study on Naphthospironone A: Construction of Benzobicyclo[3.2.1]octene Skeleton with Oxaspirocycle<\/a>, <em>Org. Lett.,&nbsp;<\/em><strong>17<\/strong>, 3746\u20133749 (2015), by J. Sakata, Y. Ando, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>242.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1002\/anie.201503442\" target=\"_blank\" rel=\"noopener noreferrer\">Toward Naphthocyclinones: Doubly Connected Octaketide Dimers with a Bicyclo[3.2.1]octadienone Core by Thiolate-Mediated Cyclization<\/a>, <em>Angew. Chem. Int. Ed.,&nbsp; <\/em><strong>54<\/strong>, 9650\u20139653 (2015), by Y. Ando, S. Hori, T. Fukazawa, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>241.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.5b01172\" target=\"_blank\" rel=\"noopener noreferrer\">Dioxanone-Fused Dienes Enable Highly <i>Endo<\/i>-Selective Intramolecular Diels-Alder Reaction<\/a>, <em>Org. Lett.,&nbsp;<\/em><strong>17<\/strong>, 2756\u20132759 (2015), by Y. Aoki, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>240.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1039\/C5CC01572C\" target=\"_blank\" rel=\"noopener noreferrer\">The flavan-isoflavan rearrangement: bioinspired synthetic access to isoflavonoids <i>via<\/i> 1,2-shift-alkylation sequence<\/a>, <em>Chem. Commun.,&nbsp;<\/em><strong>51<\/strong>, 7012\u20137014 (2015), by K. Nakamura, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>239.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.3987\/COM-14-S(K)106\" target=\"_blank\" rel=\"noopener noreferrer\">Toward the Pluramycins: Route Exploration from Dihydroxyanthrone Tricyclic Platform to an Aglycon, Saptomycinone B<\/a>, <em>HeteroCycles,&nbsp;<\/em><strong>90<\/strong>, 1240\u20131253 (2015), by K. Kitamura, Y. Ando, Y. Maezawa, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>238.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1039\/c4cc06390b\" target=\"_blank\" rel=\"noopener noreferrer\">A <i>seco<\/i>-catechin cyclization approach to 4\u21926-linked catechin dimers<\/a>, <em>Chem. Commun.,&nbsp;<\/em><strong>50<\/strong>, 14371\u201314373 (2014), by G. Watanabe, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>237.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1002\/anie.201405600\" target=\"_blank\" rel=\"noopener noreferrer\">Annulation Approach to Doubly Linked (A-type) Oligocatechins: Synthesis of (+)-Procyanidin A<sub>2<\/sub> and (+)-Cinnamtannin B<sub>1<\/sub><\/a>, <em>Angew. Chem. Int. Ed.,&nbsp;<\/em><strong>53<\/strong>, 10129\u201310133 (2014), by Y. Ito, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>236.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/dx.doi.org\/10.1246\/cl.140574\" target=\"_blank\" rel=\"noopener noreferrer\">Isoxazole Platform for Polyketide Assembly: Cycloaddition of Stable Benzonitrile Oxides to Stable <i>ortho<\/i>-quinone Mono-acetals and Dehydrogenation<\/a>, <em>Chem. Lett.,&nbsp;<\/em><strong>43<\/strong>, 1607\u20131609 (2014), by H. Takikawa, Y. Hashimoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>235.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201308017\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Synthesis of the Pluramycins 2: Total Synthesis and Structure Assignment of Saptomycin B<\/a>, <em>Angew. Chem. Int. Ed.,&nbsp;<\/em><strong>53<\/strong>, 1262\u20131265 (2014), by K. Kitamura, Y. Maezawa, Y. Ando, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>234.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201308016\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Two Designed Anthrones as Enabling Platforms for Flexible Bis-<i>C<\/i>-Glycosylation<\/a>, <em>Angew. Chem. Int. Ed.,&nbsp;<\/em><strong>53<\/strong>, 1258\u20131261 (2014), by K. Kitamura, Y. Ando, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>233.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201304929\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Synthesis and Determination of the Absolute Configuration of Cavicularin by a Symmetrization\/Asymmetrization Approach<\/a>, <em>Angew. Chem. Int. Ed.,&nbsp;<\/em><strong>52<\/strong>, 10472\u201310476 (2013), by H. Takiguchi, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>232.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201301591\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Total Synthesis of the Antibiotic BE-43472<\/a>, <em>Angew. Chem. Int. Ed.,&nbsp;<\/em><strong>52<\/strong>, 6658\u20136661 (2013), by Y. Yamashita, Y. Hirano, A. Takada, H. Takikawa, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>231.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2013\/cc\/c3cc41993b#!divAbstract\" target=\"_blank\" rel=\"noopener noreferrer\">First regiocontrolled synthesis of procyanidin B6, a catechin dimer with rare connectivity: a halo-capping strategy for formation of 4,6-interflavan bonds<\/a>, <em>Chem. Commun.,&nbsp;<\/em><strong>49<\/strong>, 5210\u20135212 (2013), by G. Watanabe, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>230.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/www.nature.com\/ja\/journal\/v66\/n3\/full\/ja20132a.html\" target=\"_blank\" rel=\"noopener noreferrer\">Preparation of L-Vancosamine-related Glycosyl Donors<\/a>, <em>J. Antibiot.,&nbsp;<\/em><strong>66<\/strong>, 131\u2013139 (2013), by K. Kitamura, M. Shigeta, Y. Maezawa, Y. Watanabe, D.-S. Hsu, Y. Ando, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>229.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201209041\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">A &#8220;Hot, energized&#8221; Benzyne<\/a>, <em>Angew. Chem. Int. Ed.,&nbsp;<\/em><strong>52<\/strong>, 2655\u20132656 (2013), by R. W. Hoffmann and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>228.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/hlca.201200439\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Synthesis and Structure Revision of Goupiolone A: a Benzotropolone Natural Product<\/a>, <em>Helv. Chim. Acta,&nbsp;<\/em><strong>95<\/strong>, 2194\u20132217 (2012), by N. Fukui, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>227.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2012\/ob\/c2ob26337h#!divAbstract\" target=\"_blank\" rel=\"noopener noreferrer\">Unified approach to catechin hetero-oligomers: first total synthesis of trimer EZ-EG-CA isolated from Ziziphus jujuba<\/a>, <em>Org. Biol. Chem.,&nbsp;<\/em><strong>10<\/strong>, 7685\u20137688 (2012), by T. Yano, K. Ohmori, H. Takahashi, T. Kusumi, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>226.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2012\/cc\/c2cc33704e\" target=\"_blank\" rel=\"noopener noreferrer\">A new synthetic strategy for catechin-class polyphenols: concise synthesis of (-)-epicatechin and its 3-O-gallate<\/a>, <em>Chem. Commun.,&nbsp;<\/em><strong>48<\/strong>, 8425\u20138427 (2012), by S. Stadlbauer, K. Ohmori, F. Hattori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>225.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2012\/ob\/c2ob25423a\" target=\"_blank\" rel=\"noopener noreferrer\">Synthesis of isoxazoles en route to semi-aromatized polyketides: dehydrogenation of benzonitrile oxide-para-quinone acetal cycloadducts<\/a>, <em>Org. Bio. Chem.,&nbsp;<\/em><strong>10<\/strong>, 6003\u20136009 (2012), by Y. Hashimoto, H. Takikawa, A. Takada, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>224.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/www.benthamdirect.org\/pages\/content.php?COC\/2012\/00000016\/00000005\/0005D.SGM\" target=\"_blank\" rel=\"noopener noreferrer\">Synthetic Strategies and Tactics for Oligomeric Proanthocyanidins<\/a>, <em>Curr. Org. Chem.,&nbsp;<\/em><strong>16<\/strong>, 566\u2013577 (2012), by K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>223.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201108415\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Catalytic Generation of Arynes and Trapping by Nucleophilic Addition and Iodination<\/a>, <em>Angew. Chem. Int. Ed.,&nbsp;<\/em><strong>51<\/strong>, 3368\u20133372 (2012), by T. Hamura, Y. Chuda, Y. Nakatsuji, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>222.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.jstage.jst.go.jp\/article\/cl\/40\/10\/40_10_1198\/_article\" target=\"_blank\" rel=\"noopener noreferrer\">Ring Expansion of Cyclopropylbenzocyclobutenes En Route to Benzocycloheptenes<\/a>, <em>Chem. Lett.,&nbsp;<\/em><strong>40<\/strong>, 1198\u20131200 (2011), by N. Fukui, T. Hamura, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>221.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.jstage.jst.go.jp\/article\/cl\/40\/10\/40_10_1192\/_article\" target=\"_blank\" rel=\"noopener noreferrer\">Expeditious Modular Assembly of Multisubstituted Cyclohexanes via Dioxanone-Dienes<\/a>, <em>Chem. Lett.,&nbsp;<\/em><strong>40<\/strong>, 1192\u20131194 (2011), by Y. Aoki, T. Yoshinari, Y. Mochizuki, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>220.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.jstage.jst.go.jp\/article\/cl\/40\/10\/40_10_1069\/_article\" target=\"_blank\" rel=\"noopener noreferrer\">Concise Synthesis of Riccardin C, Macrocyclic Bisbibenzyl Natural Product<\/a>, <em>Chem. Lett.,&nbsp;<\/em><strong>40<\/strong>, 1069\u20131071 (2011), by H. Takiguchi, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>219.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402011009173\" target=\"_blank\" rel=\"noopener noreferrer\">Total synthesis and structure revision of deacetylravidomycin M<\/a>, <em>Tetrahedron,&nbsp;<\/em><strong>67<\/strong>, 6460\u20136468 (2011), by A. Ben, D.-S. Hsu, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>218.<\/td>\n<td><a class=\"blank\" href=\"https:\/\/www.jstage.jst.go.jp\/article\/cl\/40\/7\/40_7_744\/_article\" target=\"_blank\" rel=\"noopener noreferrer\">Regioselective Approach to Multisubstituted Benzenes<\/a>, <em>Chem. Lett.,&nbsp;<\/em><strong>40<\/strong>, 744\u2013746 (2011), by H. Seo, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>217.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2011\/CC\/C1CC11758K\" target=\"_blank\" rel=\"noopener noreferrer\">Domino Pericyclic Route to Polysubstituted Salicylic Acid Derivatives: Four Sequential Processes from Enynones and Ketene Silyl Acetals<\/a>, <em>Chem. Commun.,&nbsp;<\/em><strong>47<\/strong>, 6891\u20136893 (2011), by T. Hamura, S. Iwata, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>216.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/www.jstage.jst.go.jp\/article\/cl\/40\/6\/40_612\/_article\" target=\"_blank\" rel=\"noopener noreferrer\">Ring Expansion Approach to Azaspiro[4.5]decane Skeletons via Electrophilic Activation of Benzocyclobutenols Bearing Pyridyl Group<\/a>, <em>Chem. Lett., <\/em><strong>40<\/strong>, 612\u2013613 (2011)<em>, <\/em>by T. Hayashi, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>215.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.201100187\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Enantioselective Total Synthesis of (\u2013)-Euxanmodin B: Axially Chiral Natural Product with Anthraquinone\u2013Xanthone Composite Structure<\/a>, <em>Chem. Asian J<\/em>., <strong>6<\/strong>, 1752-1756 (2011), by N. Takahashi, T. Kanayama, K. Okuyama, H. Kataoka, H. Fukaya, K. Suzuki, and T. Matsumoto.<\/td>\n<\/tr>\n<tr>\n<td>214.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201007473\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Integrated Synthetic Strategy for Higher Catechin Oligomers<\/a>, <em>Angew. Chem. Int. Ed.,<\/em> <strong>50<\/strong>, 4862\u20134867 (2011), by K. Ohmori, T. Shono, Y. Hatakoshi, T. Yano, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>213.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.201000533\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Regioselective Remote Functionalization of Biaryl Framework via Tethered ortho-Quinol Intermediate<\/a>, <em>Chem. Asian J<\/em>., <strong>6<\/strong>, 355\u2013358 (2011), by Y. Koyama, H. Kataoka, K. Suzuki, T. Matsumoto.<\/td>\n<\/tr>\n<tr>\n<td>212.<\/td>\n<td><a class=\"blank\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201006528\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Total Synthesis and Absolute Stereochemistry of Seragakinone A<\/a>, <em>Angew. Chem. Int. Ed.,<\/em><strong> 50<\/strong>, 2297\u20132301 (2011), by A. Takada, Y. Hashimoto, K. Hikita, H. Takikawa, and K. Suzuki.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2 id=\"2006-2010\">2006-2010\u5e74<\/h2>\n<table class=\"color\">\n<tbody>\n<tr>\n<td>211.<\/td>\n<td>Efficient Bis-C-Aminoglycosylation toward the Synthesis of the Pluramycins, <em>Synlett, <\/em>2654\u20132659 (2010), by M. Shigeta, T. Hakamata, Y. Watanabe, K. Kitamura, Y. Ando, K. Suzuki, and T. Matsumoto.<\/td>\n<\/tr>\n<tr>\n<td>210.<\/td>\n<td>Lessons from Total Synthesis of Hybrid Natural Products, <em>Chem. Rec., <\/em><strong>10<\/strong>, 291\u2013307 (2010), by K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>209.<\/td>\n<td><em>anti<\/em>-Selective Vinylogous Aldol Reaction by Silylated Alkyldioxinone Dienolate, <em>Chem. Lett., <\/em><strong>39<\/strong>, 1042\u20131044 (2010)<em>,<\/em> by T. Yoshinari, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>208.<\/td>\n<td>Siloxy(trialkoxy)ethene Undergoes Regioselective [2+2] Cycloaddition to Ynones and&nbsp; Ynoates en route to Functionalized Cyclobutenediones, <em>Chem. Commun., <\/em><strong>46<\/strong>,5316\u20135318 (2010)<em>, <\/em>by S. Iwata, T. Hamura, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>207.<\/td>\n<td>General Synthesis of <em>epi<\/em>-Eeries catechins and Their 3-Gallates: Reverse Polarity Strategy, <em>Org. Biomol. Chem.,<\/em> <strong>8<\/strong>, 2693\u20132696 (2010), by K. Ohmori, T. Yano, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>206.<\/td>\n<td>Synthesis and Chiroptical Properties of p-Conjugated Polymer Consisting of Dihydropentahelicene Units with Axial Chirality, <i>J. Polym. Sci.: Polym. Chem<\/i>., 1844\uff0d1848 (2010), by M. Abe, K. Ohmori, K. Suzuki, T. Yamamoto.<\/td>\n<\/tr>\n<tr>\n<td>205.<\/td>\n<td>Hexaradialenes by Successive Ring Openings of Tris (alkoxy-tricyclobutabenzenes): Synthesis and Characterization, <i>Angew. Chem. Int.<\/i> <i>Ed. <\/i><b>49<\/b>, 3026\uff0d3029 (2010), by S. Shinozaki, T. Hamura, Y. Ibusuki, K. Fujii, H. Uekusa, K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>204.<\/td>\n<td>Total Synthesis and Absolute Configuration of Macrocidin A, a Cyclophane Tetramic Acid Natural Product, <i>Angew. Chem. Int.<\/i> <i>Ed<\/i>. <b>49<\/b>, 881\uff0d885 (2010), by T. Yoshinari, K. Ohmori, M. G. Schrems, A. Pfaltz, K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>203.<\/td>\n<td>Stereocontolled Synthesis of (\uff0d)-Afzelechin: General Route to Catechin-class Polyphenols by Solving an SN2 vs. SN1 Problem, <em>Chem. Lett. <\/em><b>38, <\/b>934\uff0d935 (2009),<i> <\/i>by Ken Ohmori, Megumi Takeda, Takashi Higuchi, Tomohiro Shono, and Keisuke Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>202.<\/td>\n<td>Hydrogen-Bond Control in Axially Chiral Styrenes: Selective Synthesis of Enantiomerically Pure C2-Symmetric Paracyclophanes, <em>Angew. Chem. Int. Ed.,<\/em>, <strong>48<\/strong>, 5638-5641 (2009), by K. Mori, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>201.<\/td>\n<td>Stereochemical Relay from Axially Chiral Styrene: Asymmetric Synthesis of Antibiotic, TAN-1085,<em> Angew. Chem. Int. Ed., <\/em><strong>48<\/strong>, 5633-5637 (2009), by K. Mori, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>200.<\/td>\n<td>First Stereoselective Total Synthesis of FD-594 Aglycon, <em>Angew. Chem. Int.<\/em> <em>Ed<\/em>., <strong>48<\/strong><em>, <\/em>3462-3465 (2009), by R. Masuo, K. Ohmori, L. Hintermann, S. Yoshida, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>199.<\/td>\n<td>First Total Synthesis of (+)-11-Hydroxyerythratidine, <em>Synlett<\/em>, 1041-1046 (2009), by T. Onoda, Y. Takikawa, T. Fujimoto, Y. Yasui, K. Suzuki, and T. Matsumoto.<\/td>\n<\/tr>\n<tr>\n<td>198.<\/td>\n<td>Enantio-divergent Synthesis of Tetra-Ortho-Substituted Biphenyls by Enzymatic Desymmetrization, <em>Synlett<\/em>, 941-944 (2009), by K. Okuyama, K. Shingubara, S. Tsujiyama, K. Suzuki, and T. Matsumoto.<\/td>\n<\/tr>\n<tr>\n<td>197.<\/td>\n<td>Solvent-Controlled Leaving-Group Selectivity in Aromatic Nucleophilic Substitution, <em>Org. Lett<\/em>., <strong>10<\/strong>, 4859-4862 (2008), by L. Hintermann, R. Masuo and K.Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>196.<\/td>\n<td>Isoxazole-Assisted Direct Substitution of Hydroxy Group in a-Ketols: Stereocontrolled Introduction of Angular Substituents in Polycyclic System, <em>Angew. Chem. Int.<\/em> <em>Ed<\/em>., <strong>47<\/strong>, 9887-9890 (2008), by H. Takikawa, K. Hikita and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>195.<\/td>\n<td>Formation of a-Hydroxy-b-diketones through Hydroxylation of Isoxazolium Salts: Stereoselective Approach to Angular <em>cis-<\/em>Diol in Polycyclic System,<em>Angew. Chem. Int.<\/em> <em>Ed<\/em>., <strong>47<\/strong>, 7446\uff0d7449 (2008), by H. Takikawa, A. Takada, K. Hikita, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>194.<\/td>\n<td>2,5-Dihydroxyterephthalates, 2,5-Dichloro-1,4-benzoquinone-3,6-dicarboxylates, and Polymorphic 2,5-Dichloro-3,6-dihydroxyterephthalates, <em>Synthesis, <\/em>2303\uff0d2306 (2008), by L. Hintermann, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>193.<\/td>\n<td>Linearly Fused Dicyclobutabenzenes via Dual, Regioselective Cycloadditions of 1,4-Benzdiyne Equivalent and Ketene Silyl Acetals, <em>Synlett, <\/em>1179\uff0d1184 (2008), by T. Arisawa, T. Hamura, H. Uekusa, T. Matsumoto, K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>192.<\/td>\n<td>Synthesis and Stereochemical Assignment of Angucycline Antibiotic, PD-116740, <em>Chem. Lett.,<\/em> <strong>37<\/strong>, 470\uff0d471 (2008), by K. Mori, Y. Tanaka, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>191.<\/td>\n<td>Ring Selectivity: Successive Ring Expansion of Two Benzocyclobutenes for Divergent Access to Angular and Linear Benzanthraquinone, <em>Angew. Chem. Int.<\/em> <em>Ed<\/em>., <strong>47<\/strong>, 2248\uff0d2252 (2008), T. Suzuki, T. Hamura, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>190.<\/td>\n<td>Total Synthesis and Structure Assignment of the Anthrone <em>C<\/em>-Glycoside Cassialoin, <em>Angew. Chem. Int. Ed.<\/em>, <strong>47<\/strong>, 1084\uff0d1087 (2008), by Y. Koyama, R. Yamaguchi, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>189.<\/td>\n<td>Modified Chiral Triazolium Salts for Enantioselective Benzoin Cyclization of Enolizable Keto-aldehydes: Synthesis of (+)-Sappanone B, <em>Org. Lett<\/em>., <strong>9<\/strong>, 2713\uff0d2716 (2007), by H. Takikawa and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>188.<\/td>\n<td>General Synthetic Route to Benanomicin\uff0dPradimicin Antibiotics, <em>Chem.<\/em> <em>Eur<\/em>. <em>J<\/em>., <strong>13<\/strong><em>,<\/em> 9791\uff0d9823 (2007), by M. Tamiya, K. Ohmori, M. Kitamura, T. Arai, H. Kato, M. Oorui, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>187.<\/td>\n<td>Synthesis of Highly Functionalized Isoxazoles via Base-promoted Cyclocondensation of Stable Nitrile Oxides with Active Methylene Compounds, <em>Synlett<\/em>, 2252\uff0d2256 (2007), by H. Takikawa, K. Hikita, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>186.<\/td>\n<td>Mukaiyama Aldol Reaction of Ester Acceptors: Organoaluminums Catalyze Nucleophilic Addition of Ketene Silyl Acetals, <em>Chem. Lett<\/em>., <strong>36<\/strong>, 538\uff0d539 (2007), by S. Iwata, T. Hamura, T. Matsumoto, K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>185.<\/td>\n<td>Studies on Organic Synthesis Inspired by Carbohydrates, <em>J. Synth. Org. Chem. Jpn<\/em>., <strong>65<\/strong>, 175\uff0d182 (2007), by K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>184.<\/td>\n<td>Isoxazole-directed Pinacol Rearrangement: Stereo-controlled Approach to Angular Quaternary Stereogenic Centers in Fused Polycyclic Natural Products, <em>Angew. Chem. Int. Ed., <\/em><strong>46<\/strong>, 3252\uff0d3254 (2007), by K. Suzuki, H. Takikawa, Y. Hachisu, and J. W. Bode.<\/td>\n<\/tr>\n<tr>\n<td>183.<\/td>\n<td>Stereoselective Access to Functionalized Dihydrophenathrenes via Reductive Cyclization of Biraryl Ene-Aldehydes, <em>Synlett<\/em>, 780\uff0d784 (2007), by M. Tamiya, C. Ja\u00a8ger, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>182.<\/td>\n<td>Two Isolable Conformers of Dihydropentahelicenediol Derivatives: Stereochemical Property and Its Utility for Asymmetric Reactions, <em>Chem. Lett.<\/em>, <strong>36<\/strong>, 328\uff0d329 (2007), by K. Ohmori, S. Furuya, S. Yamanoi, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>181.<\/td>\n<td>Preparation of Benzocyclobutenone Derivatives Based on Efficient Generation of Benzynes, <em>Org. Syn<\/em>., <strong>84<\/strong>, 272\uff0d284 (2007), by S. Tsujiyama and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>180.<\/td>\n<td>Concise Synthesis of (\u00b1)-\u03b3-Indomycinone, <em>Chem. Lett.<\/em>, <strong>35<\/strong>, 1016\uff0d1017 (2006), by D.-S. Hsu, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>179.<\/td>\n<td>Dodecamethoxy- and Hexaoxotricyclobutabenzene: Synthesis and Characterization, <em>J. Am. Chem. Soc.<\/em>, <strong>128<\/strong>, 10032\uff0d10033 (2006), by T. Hamura, Y. Ibusuki, H. Uekusa, T. Matsumoto, J. S. Siegel, K. K. Baldridge, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>178.<\/td>\n<td>General and Convenient Approach to Flavan-3-ols: Stereoselective Synthesis of (\uff0d)-Gallocatechin, <em>Chem. Lett.<\/em>, <strong>35<\/strong>, 1006\uff0d1007 (2006), by T. Higuchi, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>177.<\/td>\n<td>Two-Directional Annelation: Dual Benzyne Cycloadditions Starting from Bis(sulfonyloxy)diiodobenzene, <em>Angew. Chem. Int. Ed.<\/em>, <strong>45<\/strong>, 6842\uff0d6844 (2006), by T. Hamura, T. Arisawa, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>176.<\/td>\n<td>Tandem Ring Expansion of Alkenylbenzocyclobutenol Derivatives into Substituted Naphthols, <em>Angew. Chem. Int. Ed.<\/em>, <strong>45<\/strong>, 6294\uff0d6296 (2006), by T. Hamura, T. Suzuki, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>175.<\/td>\n<td>Facile One-pot Synthesis of Resorcinol Bis-<em>C<\/em>-Glycosides Possessing Two Identical Sugar Moieties, <em>Synthesis<\/em>, <strong>2006<\/strong>, 2818\uff0d2824, by T. Yamauchi, Y. Watanabe, K. Suzuki, and T. Matsumoto.<\/td>\n<\/tr>\n<tr>\n<td>174.<\/td>\n<td>Impressive Changeover of Reaction Course in Ring Expansion of Styrylbenzocyclobutenol under Alkoxide-Forming Conditions, <em>Tetrahedron Lett.<\/em>, <strong>47<\/strong>, 6677\uff0d6679 (2006), by I. Takemura, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>173.<\/td>\n<td>Convergence in [2+2+2] Synthesis of \u03b2-Phenylnaphthalene Motif in Polyaromatic Natural Products , <em>Tetrahedron Lett<\/em>., <strong>47<\/strong>, 6673\uff0d6676 (2006), by I. Takemura, K. Imura, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>172.<\/td>\n<td>Peri-selectivity in Thermolysis of Acyloxybenzocyclobutenes Possessing \u03b1,\u03b2-Unsaturated Carbonyl Group: Synthesis of 2-Bezoxin Derivatives, <em>Chem. Lett<\/em>., <strong>2006<\/strong>, 730-731, by T. Hamura, N. Kawano, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>171.<\/td>\n<td>Poly-oxygenated Tricyclobutabenzenes via Repeated [2+2] Cycloaddition of Benzyne and Ketene Silyl Acetal, <em>J. Am. Chem. Soc.<\/em>, <strong>128<\/strong>, 3534\uff0d3535 (2006), by T. Hamura, Y. Ibusuki, H. Uekusa, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>170.<\/td>\n<td>Catalytic, Enantioselective Aldehyde-Ketone Benzoin Cyclizations, <em>Angew. Chem. Int. Ed.<\/em>, <strong>45<\/strong>, 3492\uff0d3494 (2006), by H. Takikawa, Y. Hachisu, J. W. Bode, and Keisuke Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>169.<\/td>\n<td>Sc(OTf)<sub>3<\/sub>-catalyzed C-Glycosylation of \u03b2-Diketones. A Facile Access to Useful Precursors of Heteroaromatic C-Glycosides, <em>Heterocycles<\/em>, <strong>66<\/strong>, 153\uff0d160 (2006), by T. Yamauchi, M. Shigeta, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>168.<\/td>\n<td>Synthesis of L-Vancosamine Derivatives from Methyl \u03b1-D-Mannopyranoside, <em>Synlett<\/em>, <strong>2006<\/strong>, 469\uff0d471, by D.-S. Hsu, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>167.<\/td>\n<td>Bis-<i>C<\/i>-Glycosylation of Resorcinol Derivatives by an O\u2192C-Glycoside Rearrangement, <em>Synlett<\/em>, <strong>2006<\/strong>, 399\uff0d402, by T. Yamauchi, Y. Watanabe, K. Suzuki, and T. Matsumoto.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<h2 id=\"2001-2005\">2001-2005\u5e74<\/h2>\n<table class=\"color\">\n<tbody>\n<tr>\n<td>166.<\/td>\n<td>Regio- and Stereo-Controlled Total Synthesis of Benanomicin B, <em>Angew. Chem. Int. Ed<\/em>., <strong>44<\/strong>, 3871-3875 (2005), by K. Ohmori, M. Tamiya, M. Kitamura, H. Kato, M. Oorui, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>165.<\/td>\n<td>Synthesis of rac-Lotthanongine, Novel Natural Product with Flavane-Indole Hybrid Structure, <em>Synlett<\/em>, <strong>2005<\/strong>, 1311-1315, by K. Hatakeyama, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>164.<\/td>\n<td>Efficient Synthetic Route to Ravidosamine Derivatives, <em>Synlett<\/em>, <strong>2005<\/strong>, 801, by D.-S. Hsu, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>163.<\/td>\n<td>Oligomeric Catechins: Enabling Synthetic Strategy via Orthogonal Activation and C(8)-Protection, <em>Proc. Nat. Acad. Sci<\/em>., <strong>101<\/strong>, 12002-12007 (2004), by K. Ohmori, N. Ushimaru, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>162.<\/td>\n<td>Thiazolium Ylide Catalyzed Intramolecular Benzoin-Forming Reactions Substrate Scope,<em>Adv. Synth. Catalysis, <\/em><strong>346<\/strong>, 1097-1100 (2004)<em>,<\/em> by Y. Hachisu, J. W. Bode, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>161.<\/td>\n<td>Concise Three-Component Synthesis of Defucogilvocarcin M, <em>Org. Lett<\/em>., <strong>6<\/strong>, 2503-2505 (2004), by I. Takemura, K. Imura, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>160.<\/td>\n<td>Concise Total Synthesis and Structural Assignment of (+)-TAN-1085, <em>Angew. Chem., Int. Ed.,<\/em> <strong>43<\/strong>, 3167\uff0d3171 (2004), by K. Ohmori, K. Mori, Y. Ishikawa, H. Tsuruta, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>159.<\/td>\n<td>Transmission of Axial Chirality to Spiro Center Chirality, Enabling Enantiospecific Access to Erythrinan Alkaloids, <em>Synlett,<\/em><strong> 2004<\/strong>, 619\uff0d622, by Y. Yasui, K. Suzuki, and T. Matsumoto.<\/td>\n<\/tr>\n<tr>\n<td>158.<\/td>\n<td>A Novel Approach to Erythrinan Alkaloids by Utilzing Substituted Biphenyl as Building Block, <em>Synlett,<\/em><strong> 2004<\/strong>, 615\uff0d618, by Y. Yasui, Y. Koga, K. Suzuki, and T. Matsumoto.<\/td>\n<\/tr>\n<tr>\n<td>157.<\/td>\n<td>Sc(OTf)<sub>3<\/sub> as an Efficient Catalyst for Aryl <em>C<\/em>-Glycoside Synthesis, <em>Synlett, <\/em><strong>2004<\/strong>, 225\uff0d230, by A. Ben, T. Yamauchi, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>156.<\/td>\n<td>Cationic Zirconocene- or Hafnocene-Based Lewis Acids in Organic Synthesis: Glycoside\uff0dFlavonoid Analogy, <em>Tetrahedron<\/em>,<strong> 60<\/strong>, 1365\uff0d1373 (2004), K. Ohmori, K. Hatakeyama, H. Ohrui, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>155.<\/td>\n<td>Molecular Sieve (MS 4A) Promoted Cyclocondensation of Hindered, Aromatic Nitrile Oxides and Cyclic Diketones under Mild Conditions, <em>Synlett<\/em>, <strong>2003<\/strong>, 1746\uff0d1748, by T. Matsuura, J. Bode, Y. Hachisu, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>154.<\/td>\n<td>Strain-Induced Regioselectivities in Reactions of Benzyne Possessing Fused Four-Membered Ring, <em>Org. Lett.<\/em>, <strong>5<\/strong>, 3551\uff0d3554 (2003), by T. Hamura, Y. Ibusuki, K. Sato, T. Matsumoto, Y. Osamura, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>153.<\/td>\n<td>Catalytic Intramolecular Crossed Aldehyde\uff0dKetone Benzoin Reactions: A Novel Synthesis of Functionalized Preanthraquinones, <em>J. Am. Chem. Soc.,<\/em> <strong>125<\/strong>, 8432\uff0d8433 (2003)<em>,<\/em> by Y. Hachisu, J. W. Bode, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>152.<\/td>\n<td>Structural Incongruities of Coleophomone Natural Products: Insights by Total Synthesis of a Semi-Synthetic Derivative, <em>Tetrahedron Lett<\/em>., <strong>44<\/strong>, 3559\uff0d3563 (2003)<em>,<\/em> by J. W. Bode and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>151.<\/td>\n<td>Amine-Promoted Cyclocondensation of Highly Substituted Aromatic Nitrile Oxides with Diketones, <em>Tetrahedron Lett<\/em>., <strong>44<\/strong>, 3555\uff0d3558 (2003)<em>,<\/em> by J. W. Bode, Y. Hachisu, T. Matsuura, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>150.<\/td>\n<td>Isoxazole-Benzisoxazole Rearrangement Promoted Cascade Reactions Affording Stereodefined Polycycles, <em>Org. Lett.<\/em>, <strong>5<\/strong>, 395\uff0d398 (2003), by J. W. Bode, H. Uekusa, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>149.<\/td>\n<td>Facile Construction and Divergent Transformation of Polycyclic Isoxazoles: Direct Access to Polyketide Architectures, <em>Org. Lett.<\/em>, <strong>5<\/strong>, 391\uff0d394 (2003), by J. W. Bode, Y. Hachisu, T. Matsuura, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>148.<\/td>\n<td>Facile One-pot Procedure for Et<sub>3<\/sub>Al-promoted Asymmetric Pinacol-type Rearrangement, <em>Synthesis, <\/em>141\uff0d146 (2003), by T. Shinohara and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>147.<\/td>\n<td>Synthesis of Functionalized Biaryl Compounds via Ring Expansion of Alkenylcyclobutenones, <em>Tetrahedron Lett.<\/em>, <strong>44<\/strong>, 167\uff0d170 (2003), by T. Hamura, M. Morita, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>146.<\/td>\n<td>Single-Step Synthesis of Cyclooctadienone Derivatives by Reaction of Alkenylcyclobutenones with Alkenyllithiums, Enhanced Reactivity of 8\u03c0 Cyclization by Acetylating the Intermediary Lithium Tetraenolate, <em>Chem. Lett.<\/em>, <strong>2002<\/strong>, 1042\uff0d1043, by T. Hamura, N. Kawano, S. Tsuji, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>145.<\/td>\n<td>Stereoselective Substitution of Flavan Skeleton: Synthesis of Dryopteric Acid, <em>Tetrahedron Lett<\/em>., <strong>43<\/strong>,7753\uff0d7756 (2002), by K. Ohmori, N. Ushimaru, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>144.<\/td>\n<td>Semi-Pinacol Strategy for Constructing B-Ring of Pradimicin\uff0dBenanomycin Antibiotics, <em>Tetrahedron Lett<\/em>., <strong>43<\/strong>, 7023\uff0d7026 (2002), by K. Ohmori, M. Kitamura, Y. Ishikawa, H. Kato, M. Oorui, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>143.<\/td>\n<td>Pinacol Rearrangement of Heterocycles,<em> Tetrahedron Lett<\/em>., <strong>43<\/strong>, 6937\uff0d6940 (2002)<em>,<\/em> by T. Shinohara and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>142.<\/td>\n<td>Facile Access to Versatile Polyaromatic Building Blocks: Selectively Protected Benzocylobutenedione Derivatives via Regioselective [2+2] Cycloaddition of Benzyne and Ketene Silyl Acetal, <em>Helv. Chim. Acta, <\/em><strong>85<\/strong>, 3589\uff0d3604 (2002)<em>,<\/em> by T. Hamura, T. Hosoya, H. Yamaguchi, Y. Kuriyama, M. Tanabe, M. Miyamoto, Y. Yasui, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>141.<\/td>\n<td>Arene Analogs of the Heck Reaction, in &#8220;Handbook of Organopalladium Chemistry for Organic Synthesis&#8221;, E. Negishi, Ed., John Wiley &amp; Sons, Chapt. IV.6.1, 1471\uff0d1477, by K. Suzuki and K. Ohmori.<\/td>\n<\/tr>\n<tr>\n<td>140.<\/td>\n<td>Single-Step Synthesis of Cyclooctadienone Derivatives by Reaction of Cyclobutenones with Dienyllithium, <em>Chem Lett.<\/em>, <strong>2002<\/strong>, 748\uff0d749, by T. Hamura, S. Tsuji, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>139.<\/td>\n<td>Synthesis of Functionalized Cyclobutene Derivatives via Site-Selective S<sub>N<\/sub>2 Reaction of Dichlorocyclobutenes, Chem Lett., 2002, 746\uff0d747, by T. Hamura, M. Kakinuma, S. Tsuji, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>138.<\/td>\n<td>Cationic Zirconocene Species in Organic Synthesis, in &#8220;Titanium and Zirconium in Organic Synthesis&#8221;, I. Marek Ed., Chapter 8, pp. 282\uff0d318, Wiley\uff0dVCH (2002), by K. Suzuki, L. Hintermann, and S. Yamanoi.<\/td>\n<\/tr>\n<tr>\n<td>137.<\/td>\n<td>Stereochemical Anomaly in the Thermal Coversion of 7,8-Dioxy-7-alkenylbenzocyclobutenes to Dihydronaphthalenes, Org. Lett., 4, 1675\uff0d1678 (2002), by T. Hamura, M. Miyamoto, K. Imura, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>136.<\/td>\n<td>Synthesis of Benzocyclooctene Derivatives via Thermal Ring Expansion of Dienylbenzocyclobutenes, <em>Chem Lett.<\/em>, <strong>2002<\/strong>, 280\uff0d281, by T. Hamura, S. Tsuji, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>135.<\/td>\n<td>Synthesis of Hindered 1-Arylnaphthalene Derivatives via Ring Expansion of Benzocyclobutenones, <em>Org. Lett.<\/em>, <strong>4<\/strong>, 229\uff0d232 (2002), by T. Hamura, M. Miyamoto, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>134.<\/td>\n<td>Group-Selective Hydroalumination of Bis-Alkynyl Alcohols: Further Scope, <em>Tetrahedron Lett<\/em>., <strong>43<\/strong>,1031\uff0d1034 (2002), by K. Ohmori, Y. Hachisu, T. Suzuki, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>133.<\/td>\n<td>Facile and Highly Enantioselective Synthesis of Axially Chiral Biaryls by Enzymatic Desymmetrization, <em>Synlett, <\/em><strong>2002<\/strong>, 122\uff0d124<em>,<\/em> by T. Matsumoto, T. Konegawa, T. Nakamura, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>132.<\/td>\n<td>Lipase-Catalyzed Asymmetrization of Diacetate of <em>Meso<\/em>-2-(2-Propynyl)cyclohexane-1,2,3-triol toward the Total Synthesis of Aquayamycin,<em> Synlett, <\/em><strong>2001<\/strong>, 1650\uff0d1652, by T. Matsumoto,T.Konegawa, H. Yamaguchi, T. Nakamura, T. Sugai, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>131.<\/td>\n<td>Synthesis of (\uff0d)-Malyngolide via Group-Selective Hydroalumination of Bis-Alkynyl Alcohols, <em>Org. Lett<\/em>., <strong>3<\/strong>, 1741\uff0d1744 (2001), by T. Suzuki, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>130.<\/td>\n<td>Group-selective Hydroalumination of Bis-Alkynyl Alcohols, <em>Org. Lett<\/em>., <strong>3<\/strong>, 1057\uff0d1060 (2001), by K. Ohmori, T. Suzuki, K. Taya, T. Ohta, D. Tanabe, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>129.<\/td>\n<td>Convenient Procedure for One-Pot Conversion of Azides to <em>N<\/em>-Monomethylamines, <em>Synlett, <\/em><strong>2001<\/strong>, 1003\uff0d|1005, by H. Kato, K. Ohmori, and K. Suzuki.<\/td>\n<\/tr>\n<tr>\n<td>128.<\/td>\n<td>Alkylzirconation, <em>J. Organomet. Chem.<\/em>,<strong> 624<\/strong>, 143\uff0d150 (2001), by S. Yamanoi, K. Seki, T. Matsumoto, and K. Suzuki.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n","protected":false},"excerpt":{"rendered":"<p>2021\u5e74\u4ee5\u964d 2016-2020\u5e74 2011-2015\u5e74 2006-2010\u5e74 2001-2005\u5e74 1996-2000\u5e74 1991-1995\u5e74 1986-1990\u5e74 1978-1985\u5e74 \u8457 \u66f8 2021\u5e74\u4ee5\u964d 30 [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page.php","meta":{"_exactmetrics_skip_tracking":false,"_exactmetrics_sitenote_active":false,"_exactmetrics_sitenote_note":"","_exactmetrics_sitenote_category":0,"footnotes":""},"class_list":["post-16","page","type-page","status-publish","hentry"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages\/16","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=16"}],"version-history":[{"count":183,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages\/16\/revisions"}],"predecessor-version":[{"id":3189,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages\/16\/revisions\/3189"}],"wp:attachment":[{"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=16"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}