Issue 35, 2005

Synthesis of 1,3-dioxo-hexahydropyrido[1,2-c][1,3]diazepine carboxylates, a new bicyclic skeleton formed by ring expansion–RCM methodology

Abstract

A short and elegant synthetic pathway was developed for the synthesis of 1,3-dioxo-hexahydropyrido[1,2-c][1,3]diazepine carboxylates, a new 1,3-diazepan-2,4-dione containing bicyclic moiety, starting from pyroglutamate esters.

Graphical abstract: Synthesis of 1,3-dioxo-hexahydropyrido[1,2-c][1,3]diazepine carboxylates, a new bicyclic skeleton formed by ring expansion–RCM methodology

Supplementary files

Additions and corrections

Article information

Article type
Communication
Submitted
20 Jun 2005
Accepted
14 Jul 2005
First published
04 Aug 2005

Chem. Commun., 2005, 4477-4478

Synthesis of 1,3-dioxo-hexahydropyrido[1,2-c][1,3]diazepine carboxylates, a new bicyclic skeleton formed by ring expansionRCM methodology

N. Dieltiens, D. D. Claeys, B. Allaert, F. Verpoort and C. V. Stevens, Chem. Commun., 2005, 4477 DOI: 10.1039/B508663A

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