Markovnikov hydration of vinylcyclopropanes by oxymercuration-demercuration.
S Nishida, T Fujioka, N Shimizu
Index: Nishida,S. et al. Journal of Organometallic Chemistry, 1978 , vol. 156, p. 37 - 44
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Citation Number: 5
Abstract
Abstract Representative vinylcyclopropanes (Ia Ic) were hydrated in a Markovnikov fashion by oxymercuration-demercuration. Isolated yields of α-cyclopropyl-substituted alcohols were more than 80%. 2, 2-Diphenyl-l-vinylcyclopropane (Id) was the only olefin that produced a mixture of the expected alcohol, IId, and a rearranged product III. At 0 C, However, the amount of III was minimal (ca. 6%), and hence the Markovnikov hydration of Id was ...
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