Issue 14, 2002

A general, norbornyl based approach to anti-Bredt alkenesvia sequential RCM-fragmentation strategy

Abstract

A general protocol for the synthesis of bicyclo[n.3.1]frameworks with bridgehead double bond (anti-Bredt alkenes), from a common, readily available norbornyl precursor, involving sequential ring closure metathesis (RCM) and Wharton fragmentation is outlined.

Article information

Article type
Communication
Submitted
15 Apr 2002
Accepted
16 May 2002
First published
06 Jun 2002

Chem. Commun., 2002, 1456-1457

A general, norbornyl based approach to anti-Bredt alkenes via sequential RCM-fragmentation strategy

G. Mehta and R. S. Kumaran, Chem. Commun., 2002, 1456 DOI: 10.1039/B203580D

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