Formation and Reactions of Bicyclo [1.1. 1] pentyl-1 Cations
KB Wiberg, N McMurdie
Index: Wiberg, Kenneth B.; McMurdie, Neil Journal of the American Chemical Society, 1994 , vol. 116, # 26 p. 11990 - 11998
Full Text: HTML
Citation Number: 36
Abstract
Abstract: The ionization of 1-bicyclo [l. ll] pentyl halides was shown to initially form the 1, 3- bridged bicyclo-[lll] pentyl-1 cation. It appears to be a transition state that leads to the bicyclo [llO] butyl-1-carbinyl cation which can be trapped with azide ion and can be directly observed by NMR in SOzClF. Although the major products of solvolysis of the halides are 3- methylenecyclobutyl derivatives, the corresponding cation was calculated to have a ...
Related Articles:
[De Meijere, Armin; Ligang, Zhao; Belov, Vladimir N.; Bossi, Mariano; Noltemeyer, Matthias; Hell, Stefan W. Chemistry - A European Journal, 2007 , vol. 13, # 9 p. 2503 - 2516]
[Goh, Yi Ling; Tam, Eric K.W.; Bernardo, Paul H.; Cheong, Choon Boon; Johannes, Charles W.; William, Anthony D.; Adsool, Vikrant A. Organic Letters, 2014 , vol. 16, # 7 p. 1884 - 1887]
[Wiberg,K.B.; Connor,D.S. Journal of the American Chemical Society, 1966 , vol. 88, p. 4437 - 4441]
[Wiberg,K.B.; Connor,D.S. Journal of the American Chemical Society, 1966 , vol. 88, p. 4437 - 4441]
[Wiberg,K.B.; Connor,D.S. Journal of the American Chemical Society, 1966 , vol. 88, p. 4437 - 4441]