“…The reactions of this phosphonium ylide with alkylcyclopropylketones led to substituted dicyclopropylethenes like 518, whereas air oxidation furnished unsubstituted 1,2-dicyclopropylethene 517 (Scheme 84). 353 Wittig olefinations of appropriate carbonyl compounds with methylenetriphenylphosphorane and with 515 were used to prepare 1,1-(382), 354 cis-1,2-(cis-517), and trans-1,2-dicyclopropylethene (trans-517), as well as tricyclopropylethene (519). 355,356 The mixture of diastereomeric cis-517 and trans-517 could be separated by vapor-phase chromatography.…”