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Vinyl radical cyclization in the synthesis of natural products: seychellene
Authors:Gilbert Stork  Neil H. Baine
Affiliation:Department of Chemistry Columbia University New York, New York 10027 U.S.A.
Abstract:The use of vinyl radical cyclization in the simplification of synthesis design is probed with the sesquiterpene seychellene as a target. The construction is particularly effective because of very high stereoselectivity in the alkylation of a 2,2,2-bi- cyclo-5-octene-2-one system and because of the control offered by the specific location of the double bond in the product of the vinyl radical cyclization.
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