Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/85944
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Type: Journal article
Title: Linear annelation of tricyclic quinones by site selective reaction with dienes
Author: Warrener, R.N.
Evans, D.A.C.
Russell, R.A.
Citation: Tetrahedron Letters, 1984; 25(42):4833-4836
Publisher: Pergamon Press
Issue Date: 1984
ISSN: 0040-4039
1873-3581
Statement of
Responsibility: 
Ronald N. Warrener, David A.C. Evans, Richard A. Russell
Abstract: Diels Alder reactions involving tricyclic quinones of type (3) proceed at the internal pi-bond unless the terminal pi-bond is substituted with an activating substituent, e.g. So2Ar. Thermal isomerisation of the internal adducts leads to the formation of linear but aromatised products some of which can be made to retain their bridge.
Rights: © 1984 Pergamon Press Ltd.
RMID: 0030009194
DOI: 10.1016/S0040-4039(01)81532-X
Appears in Collections:Chemistry publications

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