Synthesis of prostaglandin-F2α by conjugate addition of a cuprate reagent to 3-t-butyldimethylsilyloxytricyclo[3.2.0.02,7]heptan-6-one
Abstract
A novel synthesis of (±)-prostaglandin-F2α involves the stereospecific formation of 3-endo-t-butyldimethylsiloxytricyclo[3.2.0.02,7]heptan-6-one (3) and reaction of this strained cyclopropyl ketone with the organocuprate reagent (4).
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