Issue 31, 2013

Cu(OTf)2 catalysed [6+2] cycloaddition reaction for the synthesis of highly substituted pyrrolo[1,2-a]indoles: rapid construction of the yuremamine core

Abstract

Lewis acid catalysed [6+2] cycloaddition reaction for the synthesis of pyrrolo[1,2-a]indoles generating three contiguous stereocenters in a highly regio- and diastereoselective manner has been developed and further applied for the construction of the fully functionalized tricyclic core of yuremamine.

Graphical abstract: Cu(OTf)2 catalysed [6+2] cycloaddition reaction for the synthesis of highly substituted pyrrolo[1,2-a]indoles: rapid construction of the yuremamine core

Supplementary files

Article information

Article type
Communication
Submitted
24 Jan 2013
Accepted
26 Feb 2013
First published
26 Feb 2013

Chem. Commun., 2013,49, 3260-3262

Cu(OTf)2 catalysed [6+2] cycloaddition reaction for the synthesis of highly substituted pyrrolo[1,2-a]indoles: rapid construction of the yuremamine core

D. H. Dethe, R. Boda and S. Das, Chem. Commun., 2013, 49, 3260 DOI: 10.1039/C3CC40617B

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