Publication Type
Publication Type
Peer Reviewed Journal
Mandatory Citation Fields
Authors
Byrne, LA,Gilheany, DG;
Year
2004
Month
April
Journal
Synlett
Title
Simple syntheses of seven-membered rings via an entropy/strain reduction strategy
Status
Published
Times Cited
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ring closure carbocycles heterocycles seven-membered rings catechol DIRECT CYCLIZATION METHOD CARBON-CARBON BONDS MEDIUM-SIZED RINGS COPPER(II)-INDUCED OXYGENOLYSIS ORTHO-BENZOQUINONES MOLECULAR-OXYGEN EFFICIENT METHOD EASY ACCESS ACID CATECHOLS
Volume
-1
Issue
6
Start Page
933
End Page
943
Abstract
The straightforward four-step synthesis of unsaturated seven-membered carbocycles and heterocycles via a route starting from catechols and quinones is described. The route is based on the Perkin ring-closure reaction and was designed to alleviate the usual problems associated with the formation of medium rings. This is achieved through the presence of unsaturation in the starting material, which alleviates ring strain problems, reduces the entropy of activation and ensures that the chain ends are suitably orientated to encourage ring closure.
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ISBN / ISSN
Edition
URL
DOI Link
DOI 10.1055/s-2004-820029
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Grant Details