Epoxysilane Rearrangement Induced by a Carbanion Generated by Conjugate Addition of Enolates of Chloroacetate and α-Chloroacetamides: Formation of Functionalized Cyclopropane Derivatives
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https://figshare.com/articles/dataset/Epoxysilane_Rearrangement_Induced_by_a_Carbanion_Generated_by_Conjugate_Addition_of_Enolates_of_Chloroacetate_and_Chloroacetamides_Formation_of_Functionalized_Cyclopropane_Derivatives/3225541
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资源简介：
Reaction of an enoate bearing an epoxysilane moiety at the α-position with lithium enolate of 2-chloroacetamide afforded highly functionalized
cyclopropane derivatives via a tandem process that involves Michael addition, ring opening of the epoxide, Brook rearrangement, and
intramolecular alkylation.
创建时间：
2016-05-05
