Bimolecular displacements of iodine in reactions of dimethyl[tris(trimethylsilyl)methyl]silyl iodide with salts
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference8 articles.
1. Novel properties of some highly sterically hindered organosilicon compounds
2. Preparation of tris(trimethylsilyl)methyl (“trisyl”) derivatives of silicon
3. Reaction of tris(trimethylsilyl)methylsilicon halides with methanolic sodium methoxide. Probability of sila-olefin intermediates
4. The reactions of [tris(trimethylsilyl)methyl]silicon halides and hydrides with electrophilic reagents
5. Unimolecular solvolysis of some organosilicon perchlorates and iodides
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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. Novel nucleophilic addition to the NC bond of silicon isocyanates: conversion of some sterically hindered organosilicon isocyanates into aminosilanes;Journal of Organometallic Chemistry;1997-04
4. Reactions of the highly sterically hindered compounds (Me3Si)3CSiMe2X (X Cl, Br, I, or ONO2) with NaN3, CsF, KSCN, and KOCN in MeOH;Journal of Organometallic Chemistry;1993-11
5. Preparation and reactions of some organosilicon cyanates;Inorganica Chimica Acta;1992-08
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