Proximity Effects. XXVI. Synthesis and Stereochemistry of Bicyclo [5.1. 0] octanols
AC Cope, S Moon, CH Park
Index: Cope,A.C. et al. Journal of the American Chemical Society, 1962 , vol. 84, p. 4843 - 4849
Full Text: HTML
Citation Number: 26
Abstract
In so doing, all six of the methylcycloheptanols were prepared and their configurations Additional evidence for the assignment of configurations to endo-and exo-bicyclo [5. lO] octari-2-ol also figurations have been established. were established. has been obtained. endo-and exo-bicyclo [5.1. O] octan-2-01 have been obtained as the principal products of the solvolysis of 3-cycloocten-1-yl bro~ ylate.~.~ However, endoand exo-bicyclo [5.1. 0] ...
Related Articles:
[Wiberg,K.B.; Ashe,A.J. Journal of the American Chemical Society, 1968 , vol. 90, # 1 p. 63 - 74]
[Citron, Christian A.; Rabe, Patrick; Dickschat, Jeroen S. Journal of Natural Products, 2012 , vol. 75, # 10 p. 1765 - 1776]