The reaction of XeF 2 with trialkylvinylstannanes: scope and some mechanistic observations
MA Tius, JK Kawakami
Index: Tius, Marcus A.; Kawakami, Joel K. Tetrahedron, 1995 , vol. 51, # 14 p. 3997 - 4010
Full Text: HTML
Citation Number: 45
Abstract
The combination of a vinylstannane with xenon difluoride in the presence of silver (I) triflate results in a very rapid process leading to the corresponding vinyl fluoride. The reaction is regio-and stereospecific and does not require stoichiometric Ag (I). No evidence could be obtained of radical intermediates on the reaction pathway leading to the vinyl fluorides. A symmetrical dimer derived from the vinylstannane, which was obtained as a reaction ...
Related Articles:
[Zhang, He; Zhou, Chang-Bing; Chen, Qing-Yun; Xiao, Ji-Chang; Hong, Ran Organic Letters, 2011 , vol. 13, # 4 p. 560 - 563]
[DesMarteau, Darryl D.; Xu, Ze-Qi; Witz, Michael Journal of Organic Chemistry, 1992 , vol. 57, # 2 p. 629 - 635]
[Inbasekaran, Muthiah; Peet, Norton P.; McCarthy James R.; LeTourneau, Michael E. Journal of the Chemical Society, Chemical Communications, 1985 , # 10 p. 678 - 679]
[DesMarteau, Darryl D.; Xu, Ze-Qi; Witz, Michael Journal of Organic Chemistry, 1992 , vol. 57, # 2 p. 629 - 635]
[Bornstein,J. et al. Journal of the American Chemical Society, 1963 , vol. 85, p. 1609 - 1615]