Application of the gold(I)-Catalyzed aldol reaction to a stereoselective synthesis of (2S, 3R, 4R, 6E)-3-Hydroxy-4-methyl-2-(methylamino)oct-6-enoic Acid ( = MeBmt), Cyclosporin's unusual amino acid-Reference-Cited by-同舟云学术

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Application of the gold(I)-Catalyzed aldol reaction to a stereoselective synthesis of (2S, 3R, 4R, 6E)-3-Hydroxy-4-methyl-2-(methylamino)oct-6-enoic Acid ( = MeBmt), Cyclosporin's unusual amino acid

Published:1989-11-01 Issue:7 Volume:72 Page:1471-1478
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Togni Antonio,Pastor Stephen D.,Rihs Grety

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference41 articles.

1. (a) ?Asymmetric Synthesis1?, Academic Press, Orlando, FL, 1985, Vol. 5.

2. (b) ?Asymmetric Catalysis?, NATO series, Martinus Nijhoff, Dordrech, 1986.

3. (c) ?Stereoselective Synthesis?, VCH, Weinheim, 1987.

4. (e) in ?Modern Synthetic Methods?, Ed. Springer, Berlin, 1989, Vol. 5, p. 115.

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