Issue 12, 2005

Synthesis of protected γ-carboxyglutamates and γ-acylglutamates by rearrangement of N,N-diacylglutamates

Abstract

A new method for γ-acylation of protected glutamic acids, involving intramolecular rearrangement of an acyl urethane, has been devised to prepare the protected γ-carboxyglutamates 7, 9 and 11 and the protected 4-acylglutamates 15 and 22 from N,N-bisurethanes or N-acyl-N-urethanes of general structure 1. When the formyl-urethane 17 was used in the reaction, then the intermediate 18 in the intramolecular rearrangement was obtained.

Graphical abstract: Synthesis of protected γ-carboxyglutamates and γ-acylglutamates by rearrangement of N,N-diacylglutamates

Supplementary files

Article information

Article type
Paper
Submitted
17 Mar 2005
Accepted
20 Apr 2005
First published
19 May 2005

Org. Biomol. Chem., 2005,3, 2327-2332

Synthesis of protected γ-carboxyglutamates and γ-acylglutamates by rearrangement of N,N-diacylglutamates

A. G. Avent, H. M. E. Duggan and D. W. Young, Org. Biomol. Chem., 2005, 3, 2327 DOI: 10.1039/B503900B

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