{"id":24,"date":"2016-10-27T16:22:39","date_gmt":"2016-10-27T07:22:39","guid":{"rendered":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/ohmorilab\/wordpress\/?page_id=24"},"modified":"2026-04-25T17:28:11","modified_gmt":"2026-04-25T08:28:11","slug":"%e6%9c%80%e8%bf%91%e3%81%ae%e7%a0%94%e7%a9%b6%e6%88%90%e6%9e%9c","status":"publish","type":"page","link":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=24","title":{"rendered":"\u6700\u8fd1\u306e\u7814\u7a76\u6210\u679c"},"content":{"rendered":"

2026\/04<\/h2>\n
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ChemistryEurope<\/em>\u8a8c\u306b”Site-Selective Oxidative Dimerization of Oxaphenalenone Scaffolds: Total Synthesis of (\u00b1)-Bacillosporin C<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2025\/11<\/h2>\n
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Chem. Asian J.<\/em>\u8a8c\u306b”Fluorinated Para<\/em>-Quinone Monoacetal: Versatile Reactivity for Constructing Functionalized Scaffolds<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2025\/10<\/h2>\n
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Chem. Lett.<\/em>\u8a8c\u306b”Synthetic study on \u03b3-rubromycin: spiroacetal formation by using photochemical reaction of 2-hydroxy-1,4-naphthoquinone<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2025\/5<\/h2>\n
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ChemistryEurope<\/em>\u8a8c\u306b”Synthetic Study on Bicyclic Pyranonaphthoquinone Natural Products: Construction of the Dioxabicyclo[3.3.1]nonene Motif<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2024\/11<\/h2>\n
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Angew. Chem. Int. Ed.<\/em>\u8a8c\u306b”\u00a0Total Syntheses of \u03b2- and \u03b3-Naphthocyclinones<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fSynfacts<\/i><\/a>\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2024\/10<\/h2>\n
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Tetrahedron Lett.<\/em>\u8a8c\u306b”\u00a0Facile synthetic route to isoxazoles from \u03b2-sulfinyl- and \u03b2-sulfonyl-cyclohexenones via regioselective nitrile oxide cycloaddition and in-situ elimination<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2024\/6<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”\u00a0One-Pot Synthesis of Functionalized Benzotropones via a Phthalide Ring-Opening\/Intramolecular Aldol Condensation Cascade<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2023\/12<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”\u00a0Total Syntheses of Sparsomycin and Sparoxomycins A1<\/sub> and A2<\/sub> via Sulfenate-Anion-Mediated Iterative C\u2013S Bond Formation<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2023\/11<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”\u00a0Diastereoselective Access to anti<\/em>-\u03b2-Hydroxy Sulfoxides from \u00adChiral Epoxides and Prochiral Sulfenate Anions: Mechanistic \u00adInsights, Scope, and Limitation<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2023\/8<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”\u00a0Study on Integrated Synthesis of Dimeric Pyranonaphthoquinones: Preparation of Versatile Synthetic Intermediate and Conversion into ent<\/em>-Hemi-actinorhodin and ent<\/em>-Hemi-\u03b3-actinorhodin<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2023\/8<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”\u00a0Stereospecific naphthoquinone photoredox reactions: Photochemical Reaction of 1,2-Naphthoquinone toward Enantioselective Synthesis of \u03b3-Rubromycin: Viability Dependence on Chromophore<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2023\/5<\/h2>\n
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Tetrahedron<\/em>\u8a8c\u306b”\u00a0Stereospecific naphthoquinone photoredox reactions: Total syntheses of spirocyclic natural products<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2022\/12<\/h2>\n
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Angew. Chem. Int. Ed.<\/em>\u8a8c\u306b”\u00a0Enantioselective Total Syntheses of Preussomerins: Control of Spiroacetal Stereogenicity by Photochemical Reaction of a Naphthoquinone through 1,6-Hydrogen Atom Transfer<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fSynfacts<\/i><\/a>\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2022\/9<\/h2>\n
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Org. Biomol. Chem.<\/em>\u8a8c\u306b”\u00a0De novo<\/em> synthesis of dimerization-ready flavan unit via<\/em> intramolecular Pummerer\/Friedel\u2013Crafts cascade<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2022\/5<\/h2>\n
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Angew. Chem. Int. Ed.\u00a0<\/em>\u8a8c\u306b”\u00a0Total Synthesis of Parameriatannin A2, a Branched Epicatechin Tetramer with Two Double Linkages<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fVery Important Paper\u3068\u3057\u3066\u53d6\u308a\u6319\u3052\u3089\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2022\/2<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”\u00a0Total Synthesis and Structure Assignment of Saptomycin H<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fEditor\u2019s Choice\u3068\u3057\u3066\u53d6\u308a\u6319\u3052\u3089\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2021\/10<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”\u00a0Group-Selective Approaches to Complex Natural Product Synthesis: Three Examples of Diastereotopos-Selective Reactions<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2021\/09<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”\u00a0Synthetic Study on Carthamin, Part 4. Improved Synthesis of a C<\/em>-Glycosyl Quinochalcone by Installation of a Side Chain through Regioselective De-O<\/em>-methylation and Acyl Rearrangement<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2021\/05<\/h2>\n
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Bull. Chem. Soc. Jpn.<\/em>\u8a8c\u306b”\u00a0Model Study toward Total Synthesis of Dimeric Pyranonaphthoquinones: Synthesis of Hemi-Actinorhodin<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306f\u512a\u79c0\u8ad6\u6587\uff08Selected Paper\uff09\u306b\u9078\u51fa\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2021\/02<\/h2>\n
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Helv. Chim. Acta<\/em>\u8a8c\u306b”\u00a0Photoredox Reaction of Naphthoquinone C<\/em>\u2010Glycoside Revisited: Insight into Stereochemical Aspect<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2021\/01<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”\u00a0Synthetic Study on Acremoxanthone A, Part 2: Model Study on the EFG Xanthone Moiety through a Nitrile Oxide Cycloaddition\u2013SN<\/sub>Ar Sequence<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2020\/09<\/h2>\n
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Chem. Lett.<\/em>\u8a8c\u306b”\u00a0Thiolate-mediated Reductive Cyclizations: Scope, Limitation and Novel Mechanistic Insights<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fEditor\u2019s Choice\u3068\u3057\u3066\u53d6\u308a\u6319\u3052\u3089\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2020\/07<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”\u00a0Synthetic Study on Lactonamycins, Part 2: Stereoselective Access to ABCD-Ring System<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2020\/04<\/h2>\n
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Angew. Chem. Int. Ed.<\/em>\u8a8c\u306b”\u00a0Intramolecular Benzyne\u2013Phenolate [4+2] Cycloadditions<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2020\/03<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”\u00a0Synthesis of Enantiopure C2<\/em>-Symmetric Anthracenophane and Dimerization En Route to Multiple-Bridged Cyclophanes<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2020\/02<\/h2>\n
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Chem. Asian J.<\/em>\u8a8c\u306b”\u00a0Toward Pluramycins with Epoxy Side Chain: Syntheses of Kidamycinone and Epoxykidamycinone (Saptomycinone H)<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2019\/12<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”\u00a0Hydroxylamine-Mediated Anthrapyranone Formation, Solving 5-exo<\/em>\/6-endo<\/em> Issue toward Synthesis of Pluramycin-Class Antibiotics<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/em><\/p><\/blockquote>\n

2019\/10<\/h2>\n
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Org. Biomol. Chem.<\/em>\u8a8c\u306b”\u00a0Syntheses of doubly linked proanthocyanidins using free flavan units as nucleophiles: insight into the origin of the high regioselectivity of annulation<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2019\/10<\/h2>\n
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Heterocycles<\/em>\u8a8c\u306b”\u00a0\u03b1-L-Vancosamine Aryl C<\/em>-Glycosides, Less Stable Anomers: A Problem in Synthesis of Pluramycin-Class Antibiotics <\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2019\/08<\/h2>\n
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Angew. Chem. Int. Ed.<\/em>\u8a8c\u306b”\u00a0Stereochemical Dichotomy in Two Competing Cascade Processes: Total Syntheses of Both Enantiomers of Spiroxin\u2005A <\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2019\/03<\/h2>\n
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Angew. Chem. Int. Ed.<\/em>\u8a8c\u306b”\u00a0Total Synthesis of Carthamin, a Traditional Natural Red Pigment <\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fHot Papers\u3068\u3057\u3066\u53d6\u308a\u6319\u3052\u3089\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2019\/03<\/h2>\n
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Angew. Chem. Int. Ed.<\/em>\u8a8c\u306b” Total Synthesis of Actinorhodin <\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2019\/03<\/h2>\n
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CHIMIA<\/em>\u8a8c\u306b” Synthesis of Oxygenated ortho-Methylbenzaldehydes via Aryne [2+2] Cycloaddition and Benzocyclobutenol Ring Opening <\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2019\/03<\/h2>\n
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Chem. Sci.<\/em>\u8a8c\u306b” 2-Bromo-6-(chlorodiisopropylsilyl)phenyl tosylate as an efficient platform for intramolecular benzyne\u2013diene [4 + 2] cycloaddition <\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2019\/01<\/h2>\n
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Synthesis<\/em>\u8a8c\u306b” General Synthetic Approach to Rotenoids via Stereospecific, Group-Selective 1,2-Rearrangement and Dual SN<\/sub>Ar Cyclizations of Aryl Fluorides <\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2018\/10<\/h2>\n
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Chem. Soc. Rev.<\/em>\u8a8c\u306b”Aryne-based strategy in the total synthesis of naturally occurring polycyclic compounds<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2018\/08<\/h2>\n
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Chem. Eur. J.<\/em>\u8a8c\u306b”Photoredox Reactions of Quinones<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2018\/06<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”Model Reactions for the Enantioselective Synthesis of \u03b3-Rubromycin: Stereospecific Intramolecular Photoredox Cyclization of an ortho-Quinone Ether to a Spiroacetal<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2018\/06<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”Total Syntheses of Pusilatins A\u2013C, Liverwort-Derived Macrocyclic Bisbibenzyl Dimers<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2018\/06<\/h2>\n
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Bioorg. Med. Chem. Lett.<\/em>\u8a8c\u306b”Intramolecular photoredox reactions of 1,2-naphthoquinone derivatives<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2018\/05<\/h2>\n
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Synthesis<\/em>\u8a8c\u306b”Total Synthesis of Bis-anthraquinone Antibiotic BE-43472B<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2018\/05<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”Total Synthesis of Selligueain A, a Sweet Flavan Trimer<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2018\/04<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”First Total Synthesis of Oxirapentyn D, a Highly Oxidized Chromene Natural Product<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2018\/04<\/h2>\n
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Chem. Rev.<\/em>\u8a8c\u306b”Total Synthesis of Aryl C<\/i>-Glycoside Natural Products: Strategies and Tactics<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2017\/08<\/h2>\n
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Angew. Chem. Int. Ed.<\/em>\u8a8c\u306b”First Total Syntheses of Tetracenomycins\u2005C and X<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fNature Reviews Chemistry<\/i><\/a>\uff0cChem-Station<\/a>\u304a\u3088\u3073Synfacts<\/i><\/a>\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2017\/08<\/h2>\n
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Angew. Chem. Int. Ed.<\/em>\u8a8c\u306b”Stereospecificity in Intramolecular Photoredox Reactions of Naphthoquinones: Enantioselective Total Synthesis of (\u2212)-Spiroxin\u2005C<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fSynfacts<\/i><\/a>\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2017\/07<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”Preparation of 2-Substituted 3-Methoxycarbonyl-4-methoxyfurans that Allow Access to Highly Functionalized Naphthalenes via Regioselective Cycloaddition with Alkoxybenzyne<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2017\/06<\/h2>\n
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Chem. Lett.<\/em>\u8a8c\u306b”Oxidative Ring Opening of Benzocyclobutenone Oximes: Novel Access to Stable Nitrile Oxides<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fEditor\u2019s Choice\u3068\u3057\u3066\u53d6\u308a\u6319\u3052\u3089\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2017\/05<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”Intramolecular Photoredox Reaction of Naphthoquinone Derivatives<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2017\/03<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”Enantioselective Access to Bicyclo[3.2.1]octadienone Skeleton: Total Syntheses of (+)-Engelharquinone and Its Epoxide<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2017\/02<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”Total Syntheses of Atrovenetin and Atrovenetinone: A Naphthalene-Annulation Approach to a Discoid Tricycle Using Allenic Acid<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2017\/02<\/h2>\n
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Org. Lett.<\/em>\u8a8c\u306b”Synthetic Study on Carthamin. 2. Stereoselective Approach to C<\/i>-Glycosyl Quinochalcone via Desymmetrization<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/12<\/h2>\n
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Angew. Chem. Int. Ed.<\/em>\u8a8c\u306b”Stereocontrolled Total Syntheses of (\u2212)-Rotenone and (\u2212)-Dalpanol by 1,2-Rearrangement and SN<\/sub>Ar Oxycyclizations<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/09<\/h2>\n
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Synlett<\/em>\u8a8c\u306b”Synthetic Study on Acremoxanthone A: Construction of Bicyclo[3.2.2]nonane CD Skeleton and Fusion of AB Rings<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fSynlett\u306e2017\u5e74\u7b2c2\u5dfb\u306e\u8868\u7d19\u306b\u9078\u51fa\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/09<\/h2>\n
\"\"<\/a><\/figure>\n

Helv. Chim. Acta<\/em>\u8a8c\u306b”Total Synthesis of the Proposed Structure of Ardimerin, and Proposal for its Structural Revision<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/08<\/h2>\n
\"\"<\/a><\/figure>\n

Org. Lett.<\/em>\u8a8c\u306b”Total Synthesis of (+)-Vicenin-2<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fEditor’s Choice\u3068\u3057\u3066\u53d6\u308a\u6319\u3052\u3089\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/08<\/h2>\n
\"\"<\/a><\/figure>\n

Bull. Chem. Soc. Jpn.<\/em>\u8a8c\u306b”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>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002\u672c\u8ad6\u6587\u306fBCSJ Award Article\u306b\u9078\u51fa\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/07<\/h2>\n
\"\"<\/a><\/figure>\n

Synthesis<\/em>\u8a8c\u306b”Synthesis of \u03b2-Hydroxynaphthoate Derivatives from Ketodioxinones via Benzyne Acyl-Alkylation and Aldol Condensation Cascade<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/07<\/h2>\n
\"\"<\/a><\/figure>\n

Synlett<\/em>\u8a8c\u306b”Synthetic Study on Carthamin: Problem and Solution for Oxidative Dearomatization Approach to Quinol\u00a0C<\/em>-Glycoside<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/06<\/h2>\n
\"\"<\/a><\/figure>\n

Synlett<\/em>\u8a8c\u306b”Facile Synthesis of Stereodefined \u03b1-Iodovinyl Sulfoxides, Versatile Platform to Trisubstituted Olefins<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/03<\/h2>\n
\"\"<\/a><\/figure>\n

Synlett<\/em>\u8a8c\u306b”First Total Synthesis of Dermocanarin 2<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n

2016\/03<\/h2>\n
\"\"<\/a><\/figure>\n

Synlett<\/em>\u8a8c\u306b”Stereocontrolled Synthesis of Planar Chiral Carba-Paracyclophanes via Modular Assembly<\/a>“\u304c\u63b2\u8f09\u3055\u308c\u307e\u3057\u305f\u3002<\/p><\/blockquote>\n","protected":false},"excerpt":{"rendered":"

2026\/04 ChemistryEurope\u8a8c\u306b”Site-Selective Oxidative Dimerization of Oxaphenalenone Scaffolds: Total Synth […]<\/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-24","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\/24","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=24"}],"version-history":[{"count":181,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages\/24\/revisions"}],"predecessor-version":[{"id":3187,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages\/24\/revisions\/3187"}],"wp:attachment":[{"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=24"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}