Issue 3, 2003

Rh2(OAc)4-catalyzed reactions of α-diazoimides: a simple and novel synthesis of mono- and bis(2,3-fused perhydrooxazol-4-one) systems

Abstract

Simply, trapping the intermediate isomünchnone 1,3-dipoles by the external oxygen nucleophiles resulted in new heterocyclic systems and the use of diols led to the formation of four carbon-oxygen bonds in a single operation which eventually delivered bis(2,3-fused perhydrooxazol-4-one) systems.

Graphical abstract: Rh2(OAc)4-catalyzed reactions of α-diazoimides: a simple and novel synthesis of mono- and bis(2,3-fused perhydrooxazol-4-one) systems

Supplementary files

Article information

Article type
Communication
Submitted
26 Nov 2002
Accepted
06 Jan 2003
First published
15 Jan 2003

Chem. Commun., 2003, 440-441

Rh2(OAc)4-catalyzed reactions of α-diazoimides: a simple and novel synthesis of mono- and bis(2,3-fused perhydrooxazol-4-one) systems

S. Muthusamy and C. Gunanathan, Chem. Commun., 2003, 440 DOI: 10.1039/B211717G

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