Synthesis of homochiral 4-amino-4-carboxy-2-phosphonomethylpyrrolidines via a diastereoselective bucherer-bergs reaction of 4-oxopyrrolidine derivative: Novel conformationally restricted AP 5 analogues-Reference-Cited by-同舟云学术

Synthesis of homochiral 4-amino-4-carboxy-2-phosphonomethylpyrrolidines via a diastereoselective bucherer-bergs reaction of 4-oxopyrrolidine derivative: Novel conformationally restricted AP 5 analogues

Published:1995-09 Issue:9 Volume:6 Page:2271-2279
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Tanaka Ken-ichi,Iwabuchi Hirokazu,Sawanishi Hiroyuki

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference24 articles.

1. Excitatory Amino Acid Transmitters

2. Exploration of phenyl-spaced 2-amino-(5-9)-phosphonoalkanoic acids as competitive N-methyl-D-aspartic acid antagonists

3. Exploration of N-phosphonoalkyl-, N-phosphonoalkenyl-, and N-(phosphonoalkyl)phenyl-spaced .alpha.-amino acids as competitive N-methyl-D-aspartic acid antagonists

4. Preferred antagonist binding state of the N-methyl-D-aspartate receptor: synthesis, pharmacology, and computer modeling of (phosphonomethyl)phenylalanine derivatives

5. Synthesis andN-Methyl-D-aspartate (NMDA) Antagonist Properties of the Enantiomers of α-Amino-5-(phosphonomethyl)[1,1′-biphenyl]-3-propanoic Acid. Use of a New Chiral Glycine Derivative

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