New enzymatic approach to the synthesis of convenient aspartic acid intermediates in peptide chemistry. Synthesis of n-benzyloxycarbonyl-l-aspartic acid β-allyl ester.-Reference-Cited by-同舟云学术

New enzymatic approach to the synthesis of convenient aspartic acid intermediates in peptide chemistry. Synthesis of n-benzyloxycarbonyl-l-aspartic acid β-allyl ester.

Published:1989-01 Issue:23 Volume:45 Page:7421-7426
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Xaus N.,Clapés P.,Bardají E.,Torres J.L.,Jorba X.,Mata J.,Valencia G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. SIDE REACTIONS IN PEPTIDE SYNTHESIS

2. SIDE REACTIONS IN PEPTIDE SYNTHESIS. VI.

3. SIDE REACTIONS IN PEPTIDE SYNTHESIS

4. FORMATION OF AMINOSUCCINYL PEPTIDES DURING ACIDOLYTIC DEPROTECTION FOLLOWED BY THEIR TRANSFORMATION TO PIPERAZINE-2, 5-DIONE DERIVATIVES IN NEUTRAL MEDIA

5. Formation of aminosuccinyl derivative from β-phenacyl aspartyl peptides catalyzed by sodium thiophenoxide

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