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A route to prostaglandin precursors from 1-(phenylthio)-2-octenyllithium.
Authors:Malcolm R Binns  Richard K Haynes  Dale E Lambert  Paul A Schober
Institution:Department of Organic Chemistry, University of Sydney, Sydney NSW 2006, Australia
Abstract:The enolates generated by the conjugate addition of 1-(phenylthio)-2-octenyllithium to 4-tert-butoxycyclopent-2-en-1-one and <-crotonolactone react with methyl 7-halohept-5-ynoates in the presence of Ph3SnCl to deliver products which may be converted into prostaglandin precursors.
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