Bromination of octmethylcyclopentene - the irregular reactivity of a sterically hindered cycloalkene
作者:Herbert Mayr、Elfriede Will、Ulrich W. Heigl、Christian Schade
DOI:10.1016/0040-4020(86)80016-3
日期:1986.1
The title compound 7 reacts with bromine under mild conditions (CCI., 20°C) to give the substitution products 9 and/or 10 an electrophilic process. The tetrabromo compound 11 is formed from 7 and bromine in refluxing CCI, a radical mechanism.
Hoffmann, H. M. R.; Vathke-Ernst, Heidrun, Chemische Berichte, 1981, vol. 114, # 8, p. 2898 - 2906
作者:Hoffmann, H. M. R.、Vathke-Ernst, Heidrun
DOI:——
日期:——
Inductive effects in neighboring-group participation. Destabilization of carbocations by CC double bonds in solvolyses of 2,2,5,5-tetramethylcyclopent-3-en-1-yl tosylates
作者:T. William Bentley、Bernhard Irrgang、Herbert Mayr、Paul v. R. Schleyer
DOI:10.1021/jo00250a015
日期:1988.7
Ungewöhnliche reaktion eines 1-cyclopropylvinyl-kations
作者:Werner Brennenstuhl、Michael Hanack
DOI:10.1016/s0040-4039(01)91040-8
日期:1984.1
Baran; Sosnicki, Polish Journal of Chemistry, 1998, vol. 72, # 12, p. 2639 - 2641