The Journal of Organic Chemistry

Thermolysis of 6-endo-(carbomethoxy) bicyclo [3.1. 0] hex-2-ene: comparison with the parent compound and effect of different thermolysis techniques

DL Garin, JS Chickos

Index: Garin, David L.; Chickos, James S. Journal of Organic Chemistry, 1980 , vol. 45, # 13 p. 2721 - 2723

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Citation Number: 5

Abstract

Thermal isomerizations of vinylcyclopropanes have been studied in great depth with regard to concerted vs. stepwise mechanisms.',* Recent interest has focused on the thermal epimerization and rearrangements of bicyclo [3.1. 0] hex-2-enes which can occur via exocyclic (C1-Cs) and endocyclic (Cl-C5) cyclopropyl hond cleavage., We investigated the thermolysis of 6-endo-(carbomethoxy) bicyclo [3.1. 01 hex-2-ene (1) in order to determine ...

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