Reaction of Phosphonate-Stabilized Carbanions with Cyclic Enones Bearing a. beta.-Leaving Group
MJ Mphahlele, TA Modro
Index: Mphahlele, Malose J.; Modro, Tomasz A. Journal of Organic Chemistry, 1995 , vol. 60, # 25 p. 8236 - 8240
Full Text: HTML
Citation Number: 31
Abstract
Reaction between a-lithiated alkylphosphonic esters and a, P-unsaturated cyclopentenones and cyclohexenones carrying a heteroatom substituent Y in the 8-position was studied. Complete chemoselectivity was observed as a function of substituent Y. For Y= OMe exclusive additionelimination at the/?-carbon was observed, yielding a, P-unsaturated d- ketophosphonates. The P-chloro-substituted substrates (Y= C1) derived from ...
Related Articles:
[Schule, Arnaud; Liang, Huan; Vors, Jean-Pierre; Ciufolini, Marco A. Journal of Organic Chemistry, 2009 , vol. 74, # 4 p. 1587 - 1597]
[Tumer, Seniz U.; Herndon, James W.; McMullen, Leonard A. Journal of the American Chemical Society, 1992 , vol. 114, # 22 p. 8394 - 8404]
[House,H.O.; Rasmusson,G.H. Journal of Organic Chemistry, 1963 , vol. 28, p. 27 - 30]