threo-3-Alkyl- and -Arylglutamic Acid Derivatives by Michael Additions of Boc-BMI Li-Enolates to 2,6-Di-t-butyl-4-methoxyphenyl Alkenoates on the Diastereoselectivity of the Coupling of Trigonal Centers Involving Heterocyclic Li-Enolates-Reference-Cited by-同舟云学术

threo-3-Alkyl- and -Arylglutamic Acid Derivatives by Michael Additions of Boc-BMI Li-Enolates to 2,6-Di-t-butyl-4-methoxyphenyl Alkenoates on the Diastereoselectivity of the Coupling of Trigonal Centers Involving Heterocyclic Li-Enolates

Published:1992-01-13 Issue:1 Volume:1992 Page:51-61
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Suzuki Keisuke,Seebach Dieter

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Reference80 articles.

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3. (α-Alkylation of α-heterosubstituted carboxylic acids without racemization

4. ?-Alkylation of Amino Acids without Racemization. Preparation of Either (S)- or (R)-?-Methyldopa from (S)-Alanine

5. [3c] – , Liebigs Ann. Chem. 1983, 1930–1936.

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