Publication Type
Peer Reviewed Journal
Mandatory Citation Fields
Byrne, LA,Gilheany, DG;
2004
April
Synlett
Simple syntheses of seven-membered rings via an entropy/strain reduction strategy
Published
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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
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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.
DOI 10.1055/s-2004-820029
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