55.

Improvement in O−C-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.