Organocuivreux vinyliques: II. Deuterolyse, iodolyse, couplage et alcoylation stereospecifiques des vinyl-cuivres

JF Normant, G Cahiez, C Chuit, J Villieras

Index: Normant,J.F. et al. Journal of Organometallic Chemistry, 1974 , vol. 77, p. 269 - 279

Full Text: HTML

Citation Number: 71

Abstract

Abstract Vinylcopper derivatives, obtained by stereospecific addition of alkylcopper compounds to 1-alkynes, are transformed with retention to various ethylenic structures; 1- deutero-1-alkenes, symmetrical conjugated dienes, 1-iodo-1-alkenes, di-or tri-substituted alkenes and primary or secondary allylic alcohols.

Related Articles:

Highly stereo-and chemoselective iron-catalyzed alkenylation of organomagnesium compounds

[Cahiez, Gerard; Avedissian, Hovsep Synthesis, 1998 , # 8 p. 1199 - 1205]

New methodology for the conversion of epoxides to alkenes

[Wu, Feng-Ling; Ross, Benjamin P.; McGeary, Ross P. European Journal of Organic Chemistry, 2010 , # 10 p. 1989 - 1998]

New methodology for the conversion of epoxides to alkenes

[Wu, Feng-Ling; Ross, Benjamin P.; McGeary, Ross P. European Journal of Organic Chemistry, 2010 , # 10 p. 1989 - 1998]

Direct and regioselective transformation of. alpha.-chlorocarbonyl compounds into alkenes and deuteroalkenes

[Barluenga, Jose; Yus, Miguel; Concellon, Jose M.; Bernad, Pablo Journal of Organic Chemistry, 1981 , vol. 46, # 13 p. 2721 - 2726]

Thermal Dehydrochlorination of Poly (vinyl chloride) Model Compounds. I.

[Boughdady, Nabil M.; Chynoweth, Kevin R.; Hewitt, David G. Australian Journal of Chemistry, 1991 , vol. 44, # 4 p. 567 - 579]

More Articles...