Asymmetrische Synthesen über heterocyclische Zwischenstufen, XXXVI. Asymmetrische Synthese von (R)-4-Amino-4-methyl-2-pentendisäuredimethylestern (β,γ-Didehydro-α-methyl-D-glutaminsäure-dimethylester) oder (R)-2,5-Dihydro-2-methyl-5-oxo-2-pyrrolcarbonsäure-methylester nach der Bislactimether-Methode. – Studien zur asymmetrischen Synthese von β,γ-Didehydroglutaminsäuren-Reference-Cited by-同舟云学术

Asymmetrische Synthesen über heterocyclische Zwischenstufen, XXXVI. Asymmetrische Synthese von (R)-4-Amino-4-methyl-2-pentendisäuredimethylestern (β,γ-Didehydro-α-methyl-D-glutaminsäure-dimethylester) oder (R)-2,5-Dihydro-2-methyl-5-oxo-2-pyrrolcarbonsäure-methylester nach der Bislactimether-Methode. – Studien zur asymmetrischen Synthese von β,γ-Didehydroglutaminsäuren

Published:1988-01-25 Issue:1 Volume:1988 Page:87-92
ISSN:0170-2041
Container-title:Liebigs Annalen der Chemie
language:de
Short-container-title:Liebigs Ann. Chem.

Author:

Schöllkopf Ulrich,Schröder Jürgen

Publisher

Wiley

Subject

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

Reference28 articles.

1. Optisch aktive α-Arylglycinester durch asymmetrische Friedel-Crafts-Alkylierung mit dem chiralen Kation des Bislactimethers voncyclo-(L-Val-Gly)

2. Optically Activeα-Arylglycine Esters by Friedel-Crafts Alkylation with the Chiral Cation of the Bislactim Ether ofcyclo-(L-Val-Gly)

3. Stereospecific alkylation of the Schiff base ester of alanine with 2-substituted-(E)- and -(Z)-vinyl bromides. An efficient synthesis of 2-methyl-(E)-3,4-didehydroglutamic acid, a potent substrate-induced irreversible inhibitor of L-glutamate-1-decarboxylase

4. THE IRREVERSIBLE INHIBITION OF BRAIN L-GLUTAMATE-I-DECARBOXYLASE BY (2RS,3E)-2-METHYL-3,4-DIDEHYDROGLUTAMIC ACID

5. , , Stereochemistry and Biological Activity of Drugs, Blackwell Scientific Publications, Oxford 1983.

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