Direct and regioselective transformation of. alpha.-chlorocarbonyl compounds into alkenes and deuteroalkenes
J Barluenga, M Yus, JM Concellon…
Index: Barluenga, Jose; Yus, Miguel; Concellon, Jose M.; Bernad, Pablo Journal of Organic Chemistry, 1981 , vol. 46, # 13 p. 2721 - 2726
Full Text: HTML
Citation Number: 20
Abstract
The successive treatment ethyl chloroacetate or chloroacetyl chloride with Grignard reagents and lithium powder leads to symmetrical terminal olefm in a regioselective manner. The best results are obtained with acid chlorides. The influence of the temperature and the reaction time on the overall yield of the process are studied; in general, yields are increased by working at low temperature (-60" C). Internally substituted olefins are obtained from a- ...
Related Articles:
[Cahiez, Gerard; Avedissian, Hovsep Synthesis, 1998 , # 8 p. 1199 - 1205]
[Wu, Feng-Ling; Ross, Benjamin P.; McGeary, Ross P. European Journal of Organic Chemistry, 2010 , # 10 p. 1989 - 1998]
[Wu, Feng-Ling; Ross, Benjamin P.; McGeary, Ross P. European Journal of Organic Chemistry, 2010 , # 10 p. 1989 - 1998]
[Boughdady, Nabil M.; Chynoweth, Kevin R.; Hewitt, David G. Australian Journal of Chemistry, 1991 , vol. 44, # 4 p. 567 - 579]
[Normant,J.F. et al. Journal of Organometallic Chemistry, 1974 , vol. 77, p. 269 - 279]