A Fast Procedure for the Preparation of Amides/Peptides from Carboxylic Acids and Azides via Two Redox Reactions: Application to the Synthesis of Methionine Enkephalin-Reference-Cited by-同舟云学术

A Fast Procedure for the Preparation of Amides/Peptides from Carboxylic Acids and Azides via Two Redox Reactions: Application to the Synthesis of Methionine Enkephalin

Published:1996-06 Issue:6 Volume:69 Page:1705-1711
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Ghosh Sunil K.,Verma Rekha,Ghosh Usha,Mamdapur Vasant R.

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj/69/6/69_6_1705/_pdf

Reference29 articles.

1. Effect of tertiary amines and amine salts on racemization in peptide synthesis

2. Zur Synthese des Glucagons, X. Darstellung der Sequenz 22–29

3. Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1‐Hydroxy‐benzotriazolen

4. 1-Hydroxy-7-azabenzotriazole. An efficient peptide coupling additive

5. Electrophilic azide transfer to chiral enolates. A general approach to the asymmetric synthesis of .alpha.-amino acids

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