Asymmetrische Synthesen über heterocyclische Zwischenstufen, XVI. Enantioselektive Synthese von α-Alkyl-α-phenylglycinen durch Alkylieren von an C-6 chiral substituierten 3,6-Dihydro-3-phenyl-2H-1,4-oxazin-2-onen-Reference-Cited by-同舟云学术

Asymmetrische Synthesen über heterocyclische Zwischenstufen, XVI. Enantioselektive Synthese von α-Alkyl-α-phenylglycinen durch Alkylieren von an C-6 chiral substituierten 3,6-Dihydro-3-phenyl-2H-1,4-oxazin-2-onen

Published:1982-11-22 Issue:11 Volume:1982 Page:1952-1970
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Hartwig Wolfgang,Schöllkopf Ulrich

Publisher

Wiley

Subject

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

Reference33 articles.

1. Asymmetric Syntheses via Heterocyclic Intermediates; XV1. Enantioselective Synthesis of (R)-(-)-β-Hydroxyvaline using L,-Valine or (S)-O,O-Dimethyl-α-methyldopa as Chiral Auxiliary Reagents

2. Biogenetic amino acid antagonists

3. Mechanisms of action of naturally occurring irreversible enzyme inhibitors

4. Suicide enzyme inactivators

5. β -Diketoester und deren Enoläther als Aminosäure-Antagonisten. On Amino Acid Antagonists: β-Diketoesters and Their Corresponding γ-Enolethers

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