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発表論文

1996-2000年

127. Synthestic Study of Aquayamycin. Part 3: First Total Synthesis, Tetrahedron Lett., 41, 8393-8396 (2000), by T. Matsumoto, H. Yamaguchi, M. Tanabe, Y. Yasui, and K. Suzuki.
126. Synthestic Study of Aquayamycin. Part 2: Synthesis of the AB Ring Fragment, Tetrahedron Lett., 41, 8389-8392 (2000), by H. Yamaguchi, T. Konegawa, M. Tanabe, T. Nakamura, T. Matsumoto, and K. Suzuki.
125. Synthestic Study of Aquayamycin. Part 1: Synthesis of 3-(Phenylsulfonyl)phthalides Possessing a b-C-Olivoside, Tetrahedron Lett., 41, 8383-8387 (2000), by T. Matsumoto, H. Yamaguchi, T. Hamura, M. Tanabe, Y. Kuriyama, and K. Suzuki.
124. Synthetic Study of Hybrid Natural Products, Ravidomycin, Pure Appl. Chem., 1783-1786 (2000), by K. Suzuki.
123. Glycosylation Study on Pradimicin-Benanomicin Antibiotics, Tetrahedron Lett., 41, 6827-6832 (2000), by H. Kato, K. Ohmori, and K. Suzuki.
122. First Total Synthesis of Astilbin, A Biologically Active Glycosyl Flavonoid isolated from Chinese Folk Medicine, Tetrahedron Lett., 41, 5537-5541 (2000), by K. Ohmori, H. Ohrui, and K. Suzuki.
121. Thermodynamic and Kinetic Properties of trans-3, 4, 5, 6-Tetramethyl-9, 10-dihydroxy-9,10-dihydrophenanthrene: Pseudo-Rotational Barriers around Biphenyl Axis, Chirality, 12, 548-550 (2000), by H. Kato, K. Ohmori, and K. Suzuki.
120. Silicon-Directed Regioselective [2+2] Cycloaddition of a-Alkoxybenzyne and Ketene Silyl Acetals, Synlett, 2000, 520-522, by T. Hosoya, T. Hamura, Y. Kuriyama, M. Miyamoto, T. Matsumoto, and K. Suzuki.
119. Total Synthesis of Ravidomycin: Revision of Absolute and Relative Stereochemistry, Tetrahedron Lett., 41, 1063-1067 (2000), by S. Futagami, Y. Ohashi, K. Imura, T. Hosoya, K. Ohmori, T. Matsumoto, and K. Suzuki.
118. Hf-Centered Lewis Acids in Organic Synthesis, H. Yamamoto ed., Handbook on Lewis Acids - Application in Organic Synthesis, Wiley-VCH, Chapt.17, by K. Suzuki and S. Yamanoi.
117. Alkylzirconation of 1-Alkynes Catalyzed by Triphenylcarbenium Tetrakis(pentafluoro)borate, Tetrahedron Lett., 40, 8407-8410 (1999), by S. Yamanoi, H. Ohrui, K. Seki, T. Matsumoto, and K. Suzuki.
116. Divergent Behavior of Cobalt-Complexed Enynyl Compounds Having a Leaving Group, Tetrahedron Lett., 40, 4563-4566 (1999), by M. Kitamura, K. Ohmori, and K. Suzuki.
115. Total Synthesis of Pradimicinone, the Common Aglycon of the Pradimicin-Benanomicin Antibiotics, Angew. Chem., Int. Ed., Engl., 38, 1229--1232 (1999), by M. Kitamura, K. Ohmori, T. Kawase, and K. Suzuki.
114. From Axial Chirality to Central Chiralities: Pinacol Cyclization of 2,2’-Biaryldicarbaldehyde en route to trans-9,10-Dihydrophenathren-9,10-diol Substructure of Pradimicin-Benanomicin Antibiotics, Angew. Chem., Int. Ed., Engl., 38, 1226-1229 (1999), by K. Ohmori, M. Kitamura, and K. Suzuki.
113. Reaction of 1-Iodoalkynes with Allylzirconiums : Generation of Alkylidene Carbenoid via Allylmetallation, Tetrahedron Lett., 40, 2793-2796 (1999), by S. Yamanoi, T. Matsumoto, and K. Suzuki.
112. Zr- and Hf-Centered Lewis Acid in Organic Synthesis, in H. Yamamoto Ed., Lewis Acid Reagents: A Practical Approach, Chapt. 10, pp. 177-184, Oxford Univ. Press (1999), by K. Suzuki.
111. Regioselectivity of MAO-Catalyzed Allylmetallation of Conjugated Enynes with Allylzirconiums, Tetrahedron Lett., 39, 9727-9730 (1998), by S. Yamanoi, T. Matsumoto, and K. Suzuki.
110. Total Synthesis of the Furaquinocins, J. Am. Chem. Soc., 120, 11633-11644 (1998), by T. Saito, T. Suzuki, C. Akiyama, T. Ochiai, K. Takeuchi, T. Matsumoto, and K. Suzuki.
109. Base-Induced Rearrangement of 2-Vinylbenzocyclobutenol into Substituted Naphthalene Derivatives, Tetrahedron Lett., 39, 4853-4856 (1998), by T. Matsumoto, T. Hamura, M. Miyamoto, and K. Suzuki.
108. Isochroman-3-ones via Site Selective Ring Opening of Benzocyclobutenone Promoted by Lithium Tetramethylpiperidide and Reaction with Aromatic Aldehydes, Tetrahedron Lett., 38, 8985-8988 (1997), T. Matsumoto, T. Hamura, Y. Kuriyama, and K. Suzuki.
107. Unusual Regioselectivity in the Reductive Coupling of Alkynes and Allenes via Hydrozirconation and Zinca-Claisen Rearrangement: Angew. Chem., Int. Ed. Engl., 36, 2469-2471 (1997), Angew. Chem., 109, 2578-2580 (1997), by K. Suzuki, T. Imai, S. Yamanoi, M. Chino, and T. Matsumoto.
106. Implication and Improvement of Stereoselective Methylenation of Chiral Aldehyde in Total Synthesis of the Furaquinocins, Tetrahedron Lett., 38, 3755-3758 (1997), by T. Saito, T. Suzuki, K. Takeuchi, T. Matsumoto, and K. Suzuki.
105. C-Glycosyl Juglone in Angucycline Synthesis: Total Synthesis of Galtamycinon, the Common Aglycon of the C-Glycosyl Naphthacenequinone-Type Angucyclines, Tetrahedron, 53, 16533-16544 (1997), by T. Matsumoto, H. Yamaguchi, and K. Suzuki.
104. MAO-Catalyzed Allylmetallation of Alkynes, Tetrahedron Lett., 38, 3031-3034 (1997), by S. Yamanoi, T. Imai, T. Matsumoto, and K. Suzuki.
103. Enantiopure Acetals of a-Alkynyl Carbonyl Compounds: Organoaluminum-Mediated 1,2-Shift of Cobalt-Complexed Alkynyl Group with Concomitant Capture by a Nucleophile, Synlett, 1997, 304-306, by K. Taya, T. Nagasawa, and K. Suzuki.
102. Synthesis of C-Aryl Glycosides, in “Preparative Carbohydrate Chemistry”, ed. by S. Hanessian, Marcel Dekker, New York, Chapt. 24, pp 527-542, by K. Suzuki and T. Matsumoto.
101. Novel Migrating Group in 1,2-Anionotropic Reactions: Cobalt-Complexation Facilitates 1,2-Shift of Alkynyl Groups, J. Am. Chem. Soc., 118, 8949-8950 (1996), by T. Nagasawa, K. Taya, M. Kitamura, and K. Suzuki.
100. Total Synthesis of C-Glycosyl Naphthacenequinone Antibiotic, Galtamycinone, Synlett, 1996, 433--434, by T. Matsumoto, H. Yamaguchi, and K. Suzuki.
99. Hydrozirconation of Allenyl Sulfide for Generating g-Thio-substituted Allylzirconium Species and its Reaction with Carbonyl Compounds, Chem. Lett., 1996, 231-232, by M. Chino, L. G. Hao, T. Matsumoto, and K. Suzuki.
98. Total Syntheses of BE-12406 A and Its C(8)-Vinyl Analog, Heterocycles, 42, 397-414 (1996), by T. Hosoya, E. Takashiro, Y. Yamamoto, T. Matsumoto, and K. Suzuki.
97. On the Stereochemistry of Aryl C-Glycosides: Unusual Behavior of Bis-TBDPS Protected Aryl C-Olivosides, Tetrahedron Lett., 37, 637-640 (1996), by T. Hosoya, Y. Ohashi, T. Matsumoto, and K. Suzuki.
96. Stereoselective Synthesis of Cyclopropanes via Homoallylic Participation, Bull. Chem. Soc. Jpn., 69, 31-39 (1996), by T. Nagasawa, Y. Handa, Y. Onoguchi, and K. Suzuki.

1991-1995年

95. Cobalt-Complexation Makes 2-(Alkynyl)propene a Good Ene Donor in Carbonyl-Ene Reaction, Synlett, 1995, 1183-1186, by T. Nagasawa, M. Kitamura, and K. Suzuki.
94. Stereoselective Synthesis of a Cyclopropane-Containing Eicosanoid, Synlett, 1995, 1023-1024, by T. Nagasawa, Y. Onoguchi, T. Matsumoto, and K. Suzuki.
93. Total Synthesis of the Gilvocarcins, J. Synth. Org. Chem. Jpn., 53, 1045-1054 (1995), by K. Suzuki, T. Matsumoto, and T. Hosoya.
92. Total Synthesis of (±)-Furaquinocin D, J. Am. Chem. Soc., 117, 10757-10758 (1995), by T. Saito, M. Morimoto, C. Akiyama, T. Matsumoto, and K. Suzuki.
91. C-Glycosylation-Cycloaddition Approach to C-Glycosylated Juglones. Versatile Intermediates in Aryl C-Glycoside Synthesis, Chem. Lett., 1995, 677-678, by T. Matsumoto, T. Sohma, H. Yamaguchi, and K. Suzuki.
90. Stereoselective Synthesis of Cyclopropanes via Homoallylic Participation, Synlett, 1995, 731-736, by T. Nagasawa, Y. Handa, Y. Onoguchi, S. Ohba, and K. Suzuki.
89. Total Synthesis of Antibiotic C104: Benzyne-Furan Cycloaddition Approach to the Angucyclines, Tetrahedron, 51, 7347-7360 (1995), by T. Matsumoto, T. Sohma, S. Kurata, H. Yamaguchi, and K. Suzuki.
88. Convenient Synthesis of Phthalides via Regioselective Baeyer-Villiger Oxidation of Benzocyclobutenones, Synlett, 1995, 635-638, by T. Hosoya, Y. Kuriyama, T. Matsumoto, and K. Suzuki.
87. Stereospecificity in [2 + 2] Cycloaddition of Benzyne and Ketene Silyl Acetal, Tetrahedron Lett., 36, 3377-3380 (1995), by T. Hosoya, T. Hasegawa, Y. Kuriyama, and K. Suzuki.
86. AgAsF6 as Safe Alternative to AgClO4 for Generating Cationic Zirconocene Complexes: Utilities in Selective C-C Bond Forming Reactions, Tetrahedron, 55, 4483-4494 (1995), by K. Suzuki, T. Hasegawa, T. Imai, H. Maeta, and S. Ohba.
85. Benzyne-Furan Cycloaddition Approach to the Angucyclines: Total Synthesis of Antibiotic C104, Synlett, 1995, 263-266, by T. Matsumoto, T. Sohma, S. Kurata, H. Yamaguchi, and K. Suzuki.
84. [2 + 2] Cycloaddition of Benzyne and Ketene Silyl Acetal as an Efficient Route to Benzocyclobutenones, Synlett, 1995, 177-179, by T. Hosoya, T. Hasegawa, Y. Kuriyama, T. Matsumoto, and K. Suzuki.
83. Unexpected Outcome of NbCl5-Promoted Sakurai Reaction: Mechanistic Implication Relevant to C4H7+ Species, Tetrahedron Lett., 36, 899-902 (1995), by H. Maeta, T. Nagasawa, Y. Handa, T. Takei, Y. Osamura, and K. Suzuki.
82. Total Synthesis of Aryl C-Glycoside Antibiotics, Pure Appl. Chem., 66, 2175-2178 (1994) by K. Suzuki.
81. First Total Synthesis of BE-12406 A, Tetrahedron Lett., 35, 4591-4594 (1994), by T. Hosoya, E. Takashiro, T. Matsumoto, and K. Suzuki.
80. Novel Lewis Acid Catalysis in Organic Synthesis, Pure Appl. Chem., 66, 1557-1564 (1994), by K. Suzuki.
79. Convenient Procedure for Selective Generation of Allylzirconocene Chlorides via Hydrozirconation of Allenes, Synlett, 1994, 359-363, by M. Chino, T. Matsumoto, and K. Suzuki.
78. Total Syntheses of the Gilvocarcins, J. Am. Chem. Soc., 116, 1004-1015 (1994), by T. Hosoya, E. Takashiro, T. Matsumoto, and K. Suzuki.
77. On the Regiochemistry of Cycloaddition of Unsymmetrical Aryne with Nitrone. Remarkable Effect of Trialkylsilyl Substituent, Synlett, 1993, 843-846, by T. Matsumoto, T. Sohma, S. Hatazaki, and K. Suzuki.
76. New Methods in Glycoside Synthesis by Using Early Transition Metal-Derived Reagent, J. Synth. Chem. Soc. Jpn., 51, 718-732 (1993), by K. Suzuki and T. Matsumoto.
75. “Dibutyltin Diperchlorate” for Activation of Glycosyl Fluoride, Carbohydr. Res., 249, 49-56 (1993), by H. Maeta, T. Matsumoto, and K. Suzuki.
74. Total Synthesis of Aryl C-Glycoside Antibiotics, In “Recent Progress in the Chemical Synthesis of Antibiotics and Related Microbial Products”, Vol. 2., G. Lukacs ed, Springer Verlag, pp 352-403, by K. Suzuki and T. Matsumoto.
73. Hydrozirconation of Allenylstannane for Generating Three-Carbon Bimetallic Species: Synthesis of (E)-1,3-Dienes from Carbonyl Compounds, Synlett, 1993, 341-343, by H. Maeta, T. Hasegawa, and K. Suzuki.
72. [3+1] Synthetic Route toward Cyclobutane/butene Derivatives Utilizing Large a-Cation-Stabilizing Effect of Cyclopropane, Synlett, 1993, 29-31, by T. Nagasawa and K. Suzuki.
71. Two- and Four-Carbon Homologation of Aldehyde by AgClO4-Catalyzed Addition of Alkoxyalkenylzirconocene Chloride, Tetrahedron Lett., 34, 341-344 (1993), by H. Maeta and K. Suzuki.
70. Specific Interaction between Lewis Acid and Organic Substrate Can Offer New Reactivities and Selectivities in Organic Synthesis, in “Organic Synthesis in Japan, Past, Present, and Future”, J. Synth. Chem. Soc. Jpn., 50th Anniversary Special Ed. (R. Noyori Ed.), pp 425-432, by K. Suzuki.
69. New and Highly (E)-Selective Synthesis of Terminal 1,3-Diene via Three-Carbon Elongation of Aldehyde, Tetrahedron Lett., 33, 5969-5972 (1992), by H. Maeta and K. Suzuki.
68. Grignard-type Reactivity of Alkenyl and Alkylzirconocene Chloride to Aldehyde: Remarkable Catalytic Acceleration Effect of AgClO4, Tetrahedron Lett., 33, 5965-5968 (1992), by H. Maeta, T. Hashimoto, T. Hasegawa, and K. Suzuki.
67. trans-1,3-Bis(diphenylphosphinoyl)cyclohexane, Acta Cryst., C48, 1710-1712 (1992), by M. Morooka, T. Hashimoto, H. Meta, T. Matsumoto, K. Suzuki, and S. Ohba.
66. Recent Progress in O-Glycoside Synthesis. Methodological Aspects, J. Synth. Chem. Soc. Jpn., 50, 378-390 (1992), by K. Suzuki, T. Nagasawa.
65. Total Synthesis and Absolute Stereochemical Assignment of (+)-Gilvocarcin M, J. Am. Chem. Soc., 114, 3568-3570 (1992), by T. Matsumoto, T. Hosoya, and K. Suzuki.
64. Synthesis of 1,3-Bis(diphenylphosphinoyl)alkanes via Double Addition of Diphenylphosphine to a,b-Unsaturated Carbonyl Compounds. Sequential 1,4- and 1,2-Addition Promoted by NbCl5-BF3-OEt2, Synlett, 1992, 340-342, by T. Hashimoto, H. Maeta, T. Matsumoto, M. Morooka, S. Ohba, and K. Suzuki
63. threo-3-Alkyl- and -Aryl-glutamic Acid Derivatives by Michael Additions of Boc-BMI Li-Enolates to 2,6-Di-t-butyl-4-methoxyphenyl Alkenoates. On the Diastereoselectivity of Coupling of Trigonal Centers Involving Heterocyclic Li-Enolates, Liebigs Ann. Chem., 1992, 51-61, by K. Suzuki and D. Seebach.
62. An Alternative Synthetic Route to the C(11)-C(17) Fragment of Mycinolide IV, Synlett, 1992, 129-130, by K. Tomooka, K. Matsumoto, K. Suzuki, and G. Tsuchihashi.
61. Lewis Acid-Promoted Reaction of Secondary Phosphines with Carbonyl Compounds: Remarkable Effect of NbCl5 in Promoting Intramolecular Oxidation-Reduction Process, Synlett, 1992, 125-128, by K. Suzuki, T. Hashimoto, H. Maeta, and T. Matsumoto.
60. New Efficient Protocol for Aryne Generation. Selective Synthesis of Differentially Protected 1,4,5-
Naphthalenetriols, Tetrahedron Lett., 32, 6735 (1991). by T. Matsumoto, T. Hosoya, M. Katsuki, K. Suzuki,
59. O-C-Glycoside Rearrangement of Resorcinol Derivatives. Versatile Intermediates in the Synthesis of Aryl C-Glycosides, Synlett, 1991, 709-712, by T. Matsumoto, T. Hosoya, and K. Suzuki.
58. Efficient Method for Introducing Vineomycin-Fridamycin-Type Side Chain. Total Synthesis of Fridamycin E, Tetrahedron Lett., 32, 5103-5106 (1991), by T. Matsumoto, H. Jona, M. Katsuki, and K. Suzuki.
57. Ortho-Metallation of Anthracene Derivative: Problem and Solution, Tetrahedron Lett., 32, 4337-4340 (1991), by T. Matsumoto, H. Kakigi, and K. Suzuki.
56. Convergent Total Synthesis of Vineomycinone B<sub>2</sub> Methyl Ester and Its C(12)-Epimer, J. Am. Chem. Soc., 113, 6982-6992 (1991), by T. Matsumoto, M. Katsuki, H. Jona, and K. Suzuki.

1986-1990年

55. Improvement in OC-Glycoside Rearrangement Approach to C-Glycosides: Use of 1-O-Acetyl Sugar as Stable but Efficient Glycosyl Donor, Tetrahedron Lett., 31, 4629-4632 (1990), by T. Matsumoto, T. Hosoya, and K. Suzuki.
54. Cp2MCl2-AgX (M=Zr, Hf): A Reagent for Glycosidation, J. Synth. Chem. Soc., Jpn., 48, 1026-1027 (1990), by K. Suzuki and T. Matsumoto.
53. Recent Development in Glycosylation Reaction, Chemistry and Chemical Industry, 43, 918-921 (1990), by K. Suzuki.
52. Stereoselective Construction of Three- and Four-Contiguous Asymmetric Centers: A novel Possibility by Alkylative Rearrangement of Epoxy Silyl Ethers, Tetrahedron Lett., 31, 3335-3338 (1990), by M. Shimazaki, M. Morimoto, and K. Suzuki.
51. 4-O-Benzyl-2,3-O-isopropylidene-L-threose: A Useful Building Block for Stereoselective Synthesis of Monosaccharides, Tetrahedron, 46, 265-276 (1990), by T. Mukaiyama, K. Suzuki, T. Yamada, and F. Tabusa.
50. Cp2ZrCl2-AgBF4 in Benzene: Reagent System for Rapid and Highly a-Selective Glycosidation of Tetra-O-benzyl-D-mannopyranosyl Fluoride, Tetrahedron Lett., 30, 6879-6882 (1989), by K. Suzuki, H. Maeta, T. Suzuki, and T. Matsumoto.
49. Synthetic Study toward Vineomycins. Synthesis of C-Aryl Glycoside Sector via Cp2HfCl2-AgClO4-Promoted Tactics to C-Aryl Glycoside Synthesis, Tetrahedron Lett., 30, 6185-6188 (1989), by T. Matsumoto, M. Katsuki, H. Jona, and K. Suzuki.
48. Stereoselective Reduction of a-Cyclopropyl Ketones and a-Cyclopropyl Aldols. Stereo-directing Effect by Trimethylsilyl Group, Tetrahedron Lett., 30, 5447-5450 (1989), by M. Shimazaki, H. Hara, and K. Suzuki.
47. Stereospecific 1,2-Rearrangement of Cyclopropyl Group. Synthesis of Chiral a-Cyclopropyl Ketones and a-Cyclopropyl Aldols, Tetrahedron Lett, 30, 5443-5446 (1989), by M. Shimazaki, H. Hara, and K. Suzuki.
46. An Improved Procedure for Metallocene-Promoted Glycosidation. Enhanced Reactivity by Use of 1:2-Ratio of Cp2HfCl2-AgClO4, Tetrahedron Lett, 30, 4853-4856 (1989), by K. Suzuki, H. Maeta, and T. Matsumoto.
45. Lactols in Stereoselection 3. Highly anti-Cram Selective 1,2-Asymmetric Induction, Tetrahedron Lett., 30, 1563-1566 (1989), by K. Tomooka, T. Okinaga, K. Suzuki, and G. Tsuchihashi.
44. Rapid O-Glycosidation of Phenols with Glycosyl Fluoride by Using the Combinational Activator, Cp2HfCl2 and AgClO4, Chem. Lett., 1989, 437-440, by T. Matsumoto, M. Katsuki, and K. Suzuki.
43. Cp2ZrCl2-AgClO4: Efficient Promoter in the Friedel-Crafts Approach to C-Aryl Glycosides, Tetrahedron Lett., 30, 833-836 (1989), by T. Matsumoto, M. Katsuki, and K. Suzuki.
42. New Approach to C-Aryl Glycosides Starting from Phenol and Glycosyl Fluoride. Lewis Acid-Catalyzed Rearrangement of O-Glycoside to C-Glycoside, Tetrahedron Lett., 29, 6935-6938 (1988), by T. Matsumoto, M. Katsuki, and K. Suzuki.
41. First Total Synthesis of Mycinamicin IV and VII. Successful Application of New Glycosidation Reaction, Tetrahedron Lett., 29, 3575-3578 (1988), by T. Matsumoto, H. Maeta, K. Suzuki, and G. Tsuchihashi.
40. New Glycosidation Reaction 2. Preparation of 1-Fluoro-D-Desosamine Derivative and its Efficient Glycosidation by the Use of Cp2HfCl2-AgClO4 as the Activator, Tetrahedron Lett., 29, 3571-3574 (1988), by K. Suzuki, H. Maeta, T. Matsumoto, and G. Tsuchihashi.
39. New Glycosidation Reaction 1. Combinational Use of Cp2HfCl2-AgClO4 for Activation of Glycosyl Fluorides and Application to Highly b-Selective Glycosidation of D-Mycinose, Tetrahedron Lett., 29, 3567-3570 (1988), by T. Matsumoto, H. Maeta, K. Suzuki, and G. Tsuchihashi.
38. Silicon-Directed Stereoselective Synthesis of 2-Vinyl-1,3-diols. Stereodivergence with and without the Silyl Group Related to the Synthesis of Avenaciolide and Isoavenaciolide, Tetrahedron, 44, 4061-4072 (1988), by K. Suzuki, M. Miyazawa, M. Shimazaki, and G. Tsuchihashi.
37. Highly Selective Acyclic Stereocontrol Based on 1,2-Rearrangement, J. Synth. Org. Chem. Jpn., 46, 365-377 (1988), by K. Suzuki.
36. Lactols in Stereoselection 2. Stereoselective Synthesis of Disubstituted Cyclic Ethers, Tetrahedron Lett., 28, 6339-6342 (1987), by K. Tomooka, K. Matsuzawa, K. Suzuki, and G. Tsuchihashi.
35. Lactols in Stereoselection 1. Highly Selective 1,4- and 1,5-Asymmetric Induction, Tetrahedron Lett., 28, 6335-6338 (1987), by K. Tomooka, T. Okinaga, K. Suzuki, and G. Tsuchihashi.
34. On the Use of Epoxy Alcohol-Aldol Rearrangement for the Stereocontrol of Quaternary Carbon Centers, Tetrahedron Lett., 28, 5891-5894 (1987), by M. Shimazaki, H. Hara, K. Suzuki, and G. Tsuchihashi.
33. Catalytic Version of Epoxy Silyl Rearrangements, Tetrahedron Lett., 28, 3515-3518 (1987), by K. Suzuki, M. Miyazawa, and G. Tsuchihashi.
32. Two-Carbon Homologation of Amides with Lithium (Triphenylsilyl)acetylide, J. Org. Chem., 52, 2929-2930 (1987), by K. Suzuki, T. Ohkuma, and G. Tsuchihashi.
31. Stereocontrolled First Total Synthesis of Mycinolide IV, Chem. Lett., 1987, 113-116, by K. Suzuki, T. Matsumoto, K. Tomooka, K. Matsumoto, and G. Tsuchihashi.
30. Stereo-Divergent Asymmetric Total Synthesis of Avenaciolide and Isoavenaciolide. Complete Reversal of Stereoselectivity in Reduction of 2-Vinyl Aldols with / without Trimethylsilyl Directing Group, Tetrahedron Lett., 27, 6237-6240 (1986), by K. Suzuki, M. Miyazawa, M. Shimazaki, and G. Tsuchihashi.
29. Synthesis of 2-Vinyl-1,3-diols via Highly Stereoselective Reduction of 2-Vinyl Aldols using Trimethylsilyl Group as Stereo-Directing Group, Tetrahedron Lett., 27, 6233-6336 (1986), by K. Suzuki, M. Shimazaki, and G, Tsuchihashi.
28. Stereocontrolled Asymmetric Total Synthesis of Protomycinolide IV, J. Am. Chem. Soc., 108, 5221-5229 (1986), by K. Suzuki, K. Tomooka, E. Katayama, T. Matsumoto, and G. Tsuchihashi.
27. C(2)-Stereocontrol of d-Lactones via Acid-Catalyzed Cyclization of Ketene Dithioacetal Having an Internal Hydroxyl Group, Tetrahedron Lett., 27, 3661-3664 (1986), by K. Suzuki, T. Masuda, Y. Fukazawa, and G. Tsuchihashi.
26. Epoxy Silyl Ether Rearrangements: A New, Stereoselective Approach to the Synthesis of b-Hydroxy Carbonyl Compounds, J. Am. Chem. Soc., 108, 3827-3829 (1986), by K. Maruoka, M. Hasegawa, H. Yamamoto, K. Suzuki, M. Shimazaki, and G. Tsuchihashi.
25. Asymmetric Synthesis of Chiral Synthons Bearing Alkynyl Group via Organoaluminum-Promoted Pinacol-Type Rearrangement, Tetrahedron Lett., 27, 373-376 (1986), by K. Suzuki, T. Ohkuma, M. Miyazawa, and G. Tsuchihashi.

1978-1985年

24. Conformational Effects in Organoaluminum-Promoted Pinacol-Type Rearrangement, Tetrahedron Lett., 26, 4781-4784 (1985), by K. Suzuki, K. Tomooka, M. Shimazaki, and G. Tsuchihashi.
23. Stereoselective Synthesis of C(1)-C(9) and C(11)-C(17) Fragments of Protomycinolide IV Based on Asymmetric Pinacol-Type Rearrangement, Tetrahedron Lett., 26, 3711-3714 (1985), by K. Suzuki, K. Tomooka, T. Matsumoto, E. Katayama, and G. Tsuchihashi.
22. Highly Stereoselective Approach to Chiral Building Block Possessing Three Contiguous Asymmetric Centers. Preparation of Four Possible Diastereomers of b,b’-Dimethyl-bis-homoallylic Alcohol Derivative, Tetrahedron Lett., 26, 3707-3710 (1985), by K. Suzuki, E. Katayama, K. Tomooka, T. Matsumoto, and G. Tsuchihashi.
21. Enantio- and Diastereo-Controlled Synthesis of (+)- and (-)-Eldanolide Based on Asymmetric Pinacol-Type Rearrangement, Tetrahedron Lett., 26, 861-864 (1985), by K. Suzuki, T. Ohkuma, and G. Tsuchihashi.
20. Completely Stereospecific 1,2-Migration of Alkyl Groups in Et2AlCl Promoted Pinacol-Type Rearrangement, Tetrahedron Lett., 25, 4253-4256 (1984), by G. Tsuchihashi, K. Tomooka, and K. Suzuki.
19. Reductive Pinacol-Type Rearrangement of a-Mesyloxy Ketones Promoted by Organoaluminum Compounds, Tetrahedron Lett., 25, 3715-3718 (1984), by K. Suzuki, E. Katayama, T. Matsumoto, and G. Tsuchihashi.
18. Enantio- and Diastereomerically Pure threo-Homoallylic Alcohols via Highly Stereoselective Reduction of a-Methyl-b,g-unsaturated Ketones, Tetrahedron Lett., 25, 2479-2482 (1984), by K. Suzuki, E. Katayama, and G. Tsuchihashi.
17. Asymmetric Synthesis of Optically Pure a-Methyl-b,g-unsaturated Ketones via Triethylaluminum-Mediated Stereospecific Pinacol Rearrangement of Alkenyl Groups, Tetrahedron Lett., 25, 1817-1820 (1984), by K. Suzuki, E. Katayama, and G. Tsuchihashi.
16. A Formal Total Synthesis of Polyoxin J Using 4-O-Benzyl-2,3-O-isopropyliden-L-threose as a Common Chiral Building Block, Chem. Lett., 1984, 405--408, by F. Tabusa, T. Yamada, K. Suzuki, and T. Mukaiyama.
15. Asymmetric Pinacol-Type Rearrangement of a-Hydroxy Methanesulfonates Promoted by Triethylaluminum. Preparation of Optically Pure a-Aryl and a-Vinyl Ketones, Tetrahedron Lett., 24, 4997-5000 (1983), by K. Suzuki, E. Katayama, and G. Tsuchihashi.
14. The Stereoselective Synthesis of 2,3-cis-Dihydroxy-g-butyrolactones by Oxidation of g-Butenolide with KMnO4-Crown Ether, Chem. Lett., 1983, 173-174, by T. Mukaiyama, F. Tabusa, and K. Suzuki.
13. Stereoselective Synthesis of L-Sugars of Biological Importance Starting from 4-O-Benzyl-2,3-O-isopropylidene-L-threose as a Chiral Building Block, Chem. Lett., 1983, 5-8, by T. Mukaiyama, T. Yamada, and K. Suzuki.
12. The Enantioselective Michael Addition of Thiols to Cycloalkenones Using (2S,4S)-2-Anilinomethyl-1-ethyl-4-hydroxypyrrolidine as Chiral Catalyst, Bull. Chem. Soc. Jpn., 55, 3277-3282 (1982), by K. Suzuki, A. Ikegawa, and T. Mukaiyama.
11. Highly Stereoselective Synthesis of a-D-Glucopyranosides by the N-Iodosuccinimide-promoted Internal Cyclization, Chem. Lett., 1982, 1525-1528, by K. Suzuki and T. Mukaiyama.
10. The Stereoselective Synthesis of L-Tagatose. An Application of Zn(II)-Mediated Highly Stereoselective Addition of 2-Furyllithium to Polyoxygenated Aldehyde, Chem. Lett., 1982, 1169-1170, by T. Mukaiyama, Y. Yuki, and K. Suzuki.
9. 4-O-Benzyl-2,3-O-isopropylidene-L-threose. A New and Useful Building Block for the Synthesis of L-Sugars, Chem. Lett., 1982, 929-932, by T. Mukaiyama, K. Suzuki, and T. Yamada.
8. Asymmetric Synthesis of Optically Active Cyclohexenol Derivatives via Highly Stereoselective Reduction of (R)-3-(pt-Butylphenylthio)cyclohexan-1-one, Chem. Lett., 1982, 899-892, by K. Suzuki, A. Ikegawa, and T. Mukaiyama.
7. A Novel Method for the Synthesis of 2-Deoxydisaccharide by Stereoselective Cyclization of the Acyclic Precursor, Chem. Lett., 1981, 683-686, by K. Suzuki and T. Mukaiyama.
6. The Stereoselective Synthesis of D-Ribulose, Chem. Lett., 1981, 1529-1532, by K. Suzuki, Y. Yuki, and T. Mukaiyama.
5. Highly Enantioselective Michael Addition of Thiols to 2-Cyclohexenone by Using (2S,4S)-2-(Anilinomethyl)-1-ethyl-4-hydroxypyrrolidine as a Chiral Catalyst, Chem. Lett., 1981, 165-168, by T. Mukaiyama, A. Ikegawa, and K. Suzuki.
4. Asymmetric Addition of Acetylide to Aliphatic Aldehydes. Preparation of Optically Active 5-Octyl-2(5H)-furanone, Chem. Lett., 1980, 255-256, by T. Mukaiyama and K. Suzuki.
3. Enantioselective Addition of Acetylene to Aldehyde. Preparation of Optically Active Alkynyl Alcohols, Chem. Lett., 1979, 447-448, by T. Mukaiyama, K. Suzuki, K. Soai, and T. Sato.
2. Enantioface-Differentiating (Asymmetric) Addition of Alkyllithium and Dialkylmagnesium to Aldehydes by Using (2S, 2′S)-2-Hydroxymethyl-1-[(1-alkylpyrrolidin-2-yl)methyl]pyrrolidine as Chiral Ligands, J. Am. Chem. Soc., 101, 1455-1460 (1979), by T. Mukaiyama, K. Soai, T. Sato, H. Shimizu, K. Suzuki.
1. Enantioface-Differentiating (Asymmetric) Addition of Dialkylmagnesium to Aldehydes by Using (2S, 2′S)-2-Hydroxymethyl-1-[(1-alkylpyrrolidin-2-yl)methyl]pyrrolidine as a Chiral Ligands, Chem. Lett., 1978, 601-604, by T. Sato, K. Soai, K. Suzuki, T. Mukaiyama.