104858-62-0Relevant articles and documents
ANIONIC ACTIVATION OF STABILIZED YLIDES. A HIGHLY Z-STEREOSELECTIVE WITTIG REACTION OF (3-ETHOXYCARBONYL-2-OXOPROPYLIDENE)TRIPHENYLPHOSPHORANE WITH ALIPHATIC ALDEHYDES
Pietrusiewicz, K. Michal,Monkiewicz, Jaroslaw
, p. 739 - 742 (2007/10/02)
Reaction of stabilized ylide 1 with carbonyl partners can be promoted via anionic activation of the ylide; the presence of charge is responsible for the high Z-selectivity in the direct formation of conjugated enones.