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
Full Text: HTML
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 ...
Related Articles:
Pyrolysis of Esters. XX. Pyrolysis of Cyclohexenyl Acetates1, 2
[Bailey,W.J. et al. Journal of Organic Chemistry, 1962 , vol. 27, p. 1851 - 1855]
[Kurz, Karlheinz; Plieninger, Hans Chemische Berichte, 1980 , vol. 113, # 11 p. 3666 - 3668]
[Kurz, Karlheinz; Plieninger, Hans Chemische Berichte, 1980 , vol. 113, # 11 p. 3666 - 3668]