SYNTHETIC STUDIES TOWARDS FAVELINE METHYL-ETHER
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DOI
10.1016/0040-4020(95)00240-9
Abstract
A convergent approach to faveline methyl ether based on Claisen rearrangement is delineated Thus the benzylic and allylic alcohol substrate was assembled by a Grignard reaction, and the rearrangement product was oxidized and cyclized. Double bond isomers of faveline methyl ether were obtained.