Heterolytic Fragmentations of Malortyl Tosylates: Synthetic Communications: Vol 1, No 2

Synthetic Communications

An International Journal for Rapid Communication of Synthetic Organic Chemistry

Volume 1, 1971 - Issue 2

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Abstract

Heterolytic fragmentation reactions have figured prominently in several recent multistep syntheses².,³ As part of an investigation of those reactions in which, at least formally, a stabilized carbanion serves as the electrofugal group²,⁴ we have examined a number of substituted malonic esters with the aim of effecting the following sequence:

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Heterolytic Fragmentations of Malortyl Tosylates

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Heterolytic Fragmentations of Malortyl Tosylates

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