Journal of Organometallic Chemistry

The methoxymercuration of some styrene derivatives

M Bassetti, B Floris, G Illuminati

Index: Bassetti, Mauro; Floris, Barbara; Illuminati, Gabriello Journal of Organometallic Chemistry, 1980 , vol. 202, # 4 p. 351 - 362

Full Text: HTML

Citation Number: 12

Abstract

Abstract Product analyses have been carried out and reaction rates and activation parameters determined for the methoxymercuration of some styrene derivatives and related compounds in methanol. The behaviour of α-and β-alkyl substituted styrenes generally parallels that of the similarly substituted vinylferrocenes. The anomalous reactivity of β, β- dimethylstyrenes is suggested to arise from the structural features of this compound. The ...

Related Articles:

Fritsch–Buttenberg–Wiechell rearrangement to alkynes from gem-dihaloalkenes with lanthanum metal

[Umeda, Rui; Yuasa, Takumi; Anahara, Namika; Nishiyama, Yutaka Journal of Organometallic Chemistry, 2011 , vol. 696, # 9 p. 1916 - 1919]

Methyl group migration in the reactions of alkynyltrialkylborates

[Tetrahedron Letters, , vol. 29, # 33 p. 4181 - 4184]

Methyl group migration in the reactions of alkynyltrialkylborates

[Tetrahedron Letters, , vol. 29, # 33 p. 4181 - 4184]

Methyl group migration in the reactions of alkynyltrialkylborates

[Tetrahedron Letters, , vol. 29, # 33 p. 4181 - 4184]

Regioselectivity of Intermolecular Pauson–Khand Reaction of Aliphatic Alkynes: Experimental and Theoretical Study of the Effect of Alkyne Polarization

[Liu, Yan-Yun; Yang, Xu-Heng; Huang, Xiao-Cheng; Wei, Wen-Ting; Song, Ren-Jie; Li, Jin-Heng Journal of Organic Chemistry, 2013 , vol. 78, # 20 p. 10421 - 10426]

More Articles...