Herstellung enantiomerenreinercis- odertrans-konfigurierter 2-(tert-Butyl)-3-methylimidazolidin-4-one aus den Aminosäuren (S)-Alanin, (S)-Phenylalanin, (R)-Phenylglycin, (S)-Methionin und (S)-Valin-Reference-Cited by-同舟云学术

Herstellung enantiomerenreinercis- odertrans-konfigurierter 2-(tert-Butyl)-3-methylimidazolidin-4-one aus den Aminosäuren (S)-Alanin, (S)-Phenylalanin, (R)-Phenylglycin, (S)-Methionin und (S)-Valin

Published:1985-02-13 Issue:1 Volume:68 Page:135-143
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:en
Short-container-title:HCA

Author:

Naef Reto,Seebach Dieter

Publisher

Wiley

Subject

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

Reference30 articles.

1. Enantioselective Generation and Diastereoselective Reactions of Chiral Enolates Derived from ?-Heterosubstituted Carboxylic Acids. Preliminary Communication

2. Synthesis of enantiomerically enriched atrolactic acid and other α-hydroxy acids

3. Alkylation of amino acids without loss of the optical activity: preparation of .alpha.-substituted proline derivatives. A case of self-reproduction of chirality

4. R. Naef D. Seebach Justus Liebigs Ann. Chem. 1983 1930

5. α-Alkylation of a cysteine derivative without racemization and without the use of a chiral auxiliary

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