Synthesis of 3-cyclopentenols by alkoxy-accelerated vinylcyclopropane rearrangement

RL Danheiser, C Martinez-Davila…

Index: Danheiser, Rick L.; Martinez-Davila, Carlos; Morin, John M. Journal of Organic Chemistry, 1980 , vol. 45, # 7 p. 1340 - 1341

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Citation Number: 63

Abstract

The intervention of side reactions further limits the scope of the thermal vinylcyclopropane rearrangement. Cyclo- propanes bearing syn vinyl and CH groups are subject to homo- [ 1,5]-sigmatropic hydrogen migration and rarely undergo satisfactory vinylcyclopropane rearrangment.3i4 Activation energies for homo [ 1,5] hydrogen shifts are typically 31-33 kcal/mol, significantly lower than the 48-52 kcal/mol required for normal thermal ...