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1978-1985
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-(p-t-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.