Abstract
Previously studied highly stereoselective additions of Grignard, organolithium, and hydride reagents to the 2-benzoyl derivative of compound 1a have been extended to other 2-alkanoyl derivatives (1,R'=methyl, ethyl, isopropyl) and to the 2-benzoyl derivative with R=methyl. High diastereoselectivity is attained in most of the products
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