N,O Highly Regio- and Stereoselective Alkylation of Nucleophilic Glycine Equivalents with Carbonates of Allylic α-Hydroxyphosphonates: A Convenient Route to Racemic 2-Amino-5-phosphono-4-pentenoic Acids-Reference-Cited by-同舟云学术

N,O Highly Regio- and Stereoselective Alkylation of Nucleophilic Glycine Equivalents with Carbonates of Allylic α-Hydroxyphosphonates: A Convenient Route to Racemic 2-Amino-5-phosphono-4-pentenoic Acids

Published:1997-07 Issue:7 Volume:1997 Page:1437-1445
ISSN:0947-3440
Container-title:Liebigs Annalen
language:en
Short-container-title:Liebigs Ann./Recl.

Author:

Öhler Elisabeth,Kanzler Silvia

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry,General Chemistry

Reference58 articles.

1. THE EFFECTS OF A SERIES OF ω-PHOSPHONIC α-CARBOXYLIC AMINO ACIDS ON ELECTRICALLY EVOKED AND EXCITANT AMINO ACID-INDUCED RESPONSES IN ISOLATED SPINAL CORD PREPARATIONS

2. , , , , (Ciba-Geigy A.-G), EP 302 826, 1989;

3. An effective synthesis of (.+-.)-(E)-2-amino-5-phosphono-3-pentenoic acid by palladium (II)-assisted migration of the double bond.

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