Literature DB >> 16136256

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

Nicolai Dieltiens1, Diederica D Claeys, Bart Allaert, Francis Verpoort, Christian V Stevens.   

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.

Entities:  

Year:  2005        PMID: 16136256     DOI: 10.1039/b508663a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  A general enantioselective route to the chamigrene natural product family.

Authors:  David E White; Ian C Stewart; Brinton A Seashore-Ludlow; Robert H Grubbs; Brian M Stoltz
Journal:  Tetrahedron       Date:  2010-03-26       Impact factor: 2.457

2.  Synthesis of pyrrolo[1,3]diazepines by a dipolar cycloaddition - retro-Mannich domino reaction.

Authors:  Mary Liang; Cecilia Saiz; Chiara Pizzo; Peter Wipf
Journal:  Tetrahedron Lett       Date:  2009-12-01       Impact factor: 2.415

  2 in total

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