Effects of the substituents Y in reactions of compounds of the type (Me3Si)3CSiH(C6H4Y-p)I. Evidence against the SN2(intermediate) mechanism for methanolysis of (Me3Si)3CSiMe2I and (Me3Si)3CSiHPhI-Reference-Cited by-同舟云学术

Effects of the substituents Y in reactions of compounds of the type (Me3Si)3CSiH(C6H4Y-p)I. Evidence against the SN2(intermediate) mechanism for methanolysis of (Me3Si)3CSiMe2I and (Me3Si)3CSiHPhI

Published:1987-07 Issue:3 Volume:328 Page:255-262
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Azarian Davoud B.,Eaborn Colin,Lickiss Paul D.

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference27 articles.

1. Novel properties of some highly sterically hindered organosilicon compounds

2. The reactions of [tris(trimethylsilyl)methyl]silicon halides and hydrides with electrophilic reagents

3. The reactions of tris(trimethylsilyl)silicon iodides and hydrides with iodine monochloride

4. Reactions of some sterically-hindered organosilicon hydrides and iodides with halogens

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1. Direct displacement of chlorine or iodine in reactions of (Me3Si)3CSiRR′X with metal salts;Journal of Organometallic Chemistry;2000-04

2. Comparison of the reactivities of (Me3Si)3CSiMe2I and (PriMe2Si) 3CSiMe2I;Journal of Organometallic Chemistry;1997-09

3. Preparation and reactions of some organosilicon cyanates;Inorganica Chimica Acta;1992-08

4. Anchimeric assistance by γ-aryl groups in reactions of organosilicon iodides;J. Chem. Soc., Perkin Trans. 2;1992

5. Dalton perspectives. Do R3Si+ ions exist in solution?;Journal of the Chemical Society, Dalton Transactions;1992