Asymmetrische nucleophile Acylierung via metallierte chirale Aminocyanide; enantioselektive Synthese von 3-substituierten 4-Oxoestern durch asymmetrische Michael-Addition-Reference-Cited by-同舟云学术

Asymmetrische nucleophile Acylierung via metallierte chirale Aminocyanide; enantioselektive Synthese von 3-substituierten 4-Oxoestern durch asymmetrische Michael-Addition

Published:1990-02 Issue:2 Volume:102 Page:226-228
ISSN:0044-8249
Container-title:Angewandte Chemie
language:de
Short-container-title:Angew. Chem.

Author:

Enders Dieter,Gerdes Peter,Kipphardt Helmut

Publisher

Wiley

Subject

General Medicine

Reference63 articles.

1. Benzylation and Related Alkylations of α-Dimethylaminophenylacetonitrile by Means of Alkali Amides. Dehydrocyanation of Products to Form Enamines1

2. Conjugate addition of α-Dimethylaminophenylacetonitrile with Benzalacetophenone and Ethyl Cinnamate by Means of Potassium Amide1

3. Alkylations of α-Dimethylaminophenylacetonitriles and Hydrolysis to Desoxybenzoins1

4. Reactions of acyl anion equivalents derived from cyanohydrins, protected cyanohydrins and α-dialkylaminonitriles

5. (b) (Hrsg.): Umpoled Synthons, Wiley, New York 1987.

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