New amino acids derived from L-pyroglutamic acid: Synthesis of Trans-4-benzyl-cis-5-phenyl-L-proline, L-α-(2-benzyl-3-phenylpropyl)-glycine and L-α-(3-phenylpropyl)-glycine-Reference-Cited by-同舟云学术

New amino acids derived from L-pyroglutamic acid: Synthesis of Trans-4-benzyl-cis-5-phenyl-L-proline, L-α-(2-benzyl-3-phenylpropyl)-glycine and L-α-(3-phenylpropyl)-glycine

Published:1998-02 Issue:9 Volume:54 Page:1753-1762
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Van Betsbrugge Jo,Van Den Nest Wim,Verheyden Patricia,Tourwé Dirk

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Synthesis of α-phenyl proline derivatives via 1,3-dipolar cycloaddition of chiral stabilised azomethine ylids

2. A convenient synthesis of protected (R)-α-phenylproline derivatives using the Mitsunobu reaction

3. Synthesis of Enantiomerically Pure 4-Substituted Glutamic Acids and Prolines: General Aldol Reaction of Pyroglutamate Lactam Lithium Enolate Mediated by Et2O.cntdot.BF3

4. Synthesis of enantiopure .delta.-oxo .alpha.-amino esters and prolines via acylation of N-(phenylfluorenyl)glutamate enolates

5. Syntheses of proline analogs as potential mechanism-based inhibitors of proline dehydrogenase: 4-methylene-L-, (E)- and (Z)-4-(fluoromethylene)-L-, cis- and trans-5-ethynyl-(.+-.)-, and cis- and trans-5-vinyl-L-proline

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