Tetrahedron letters

The stereoselective alkylation and conformational analysis of 15-hexadecanolide

RJ Graham, L Weiler

Index: Graham, Ronald J.; Weiler, Larry Tetrahedron Letters, 1991 , vol. 32, # 8 p. 1027 - 1030

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Citation Number: 12

Abstract

Abstract 15-Hexadecanolide can be alkylated with 80% stereoselectivity. The stereochemistry of the major product was proven by chemical correlation with the alkylation products of cyclopentadecanone. A simple model using [4444] conformation of cyclohexadecane is proposed to rationalize these results along with molecular mechanics calculations.