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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. |
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