Reactions of the highly sterically hindered compounds (Me3Si)3CSiMe2X (X Cl, Br, I, or ONO2) with NaN3, CsF, KSCN, and KOCN in MeOH
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference13 articles.
1. Novel properties of some highly sterically hindered organosilicon compounds
2. Reaction of tris(trimethylsilyl)methylsilicon halides with methanolic sodium methoxide. Probability of sila-olefin intermediates
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Synthesis and reactions of [tris(trimethylsilyl)methyl]ethyl dichlorosilane;Journal of Organometallic Chemistry;2005-03
2. Recent Developments in the Synthesis and Structure of Organosilanols;Chemical Reviews;2004-10-13
3. Synthesis of new highly sterically hindered organosilicon compounds via displacement reaction of TsiSiCl3;Journal of Chemical Research;2004-07
4. Unusual mechanistic pathways. The novel chemistry of compounds with tris(trimethylsilyl)methyl or related ligands on siliconElectronic supplementary information (ESI) available: a complete list of the author's publications, with titles, on compounds with trisyl or related ligands on silicon (and for comparison, on germanium or tin) or species containing trisyl-type groups not on a metal or metalloid. See http://www.rsc.org/suppdata/dt/b1/b106509m/;Journal of the Chemical Society, Dalton Transactions;2001-11-09
5. Direct displacement of chlorine or iodine in reactions of (Me3Si)3CSiRR′X with metal salts;Journal of Organometallic Chemistry;2000-04
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