Methylenecyclopropane Ring Formation/Opening Cascade for the Synthesis of Indolizines

Methylenecyclopropane Structural isomer
DOI: 10.1021/acs.joc.7b01073 Publication Date: 2017-06-01T09:15:36Z
ABSTRACT
A unique strategy toward the synthesis of polysubstituted indolizines has been developed. When 2-pyridinyl-2-(2'-bromoallyl)-1-carboxylates were treated with Cs2CO3, starting material went through a methylenecyclopropane ring formation/opening cascade, and corresponding obtained in moderate to good yield as single regioisomer.
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