Sulfonation de dérivés siliciés acétyléniques et alléniques fonctionnels

P Bourgeois, G Merault, N Duffaut, R Calas

Index: Bourgeois,P. et al. Journal of Organometallic Chemistry, 1973 , vol. 59, p. 145 - 151

Full Text: HTML

Citation Number: 13

Abstract

Abstract Sulfonating agents such as trimethylsilyl chlorosulfonate and “dioxane, SO 3”, react with silylalkynes (ΣCH 2 C CSiMe 3) in which Σ is a functional group, to yield silylacetylene sulfonates (Σ= OMe, Cl), acetylenic sulfates (Σ= OH, OSiMe 3) or SO 3 nitrogen adduct (Σ= NR 2). Allenoxysilanes Me 3 Si (Σ 1) C C C (Σ 2) OSiMe 3 yield either allenic sulfate (Σ 1= Me 3 Si, Σ 2= t-Bu) or silyl ketonic sulfonate (Σ 1= n-Bu, Σ 2= t-Bu). A mechanism is ...

Related Articles:

Universal method for trimethylsilylation of acetylenic alcohols and glycols

[Demina, Maria; Velikanov, Andrey; Medvedeva, Alevtina; Larina, Lyudmila; Voronkov, Mikhail Journal of Organometallic Chemistry, 1998 , vol. 553, # 1-2 p. 129 - 133]

(E)-3-(Trimethylsilyl)-2-propen-1-ol. An improved preparation

[Denmark, S. E.; Jones, T. K. Journal of Organic Chemistry, 1982 , vol. 47, # 23 p. 4595 - 4597]

More Articles...