Rearrangements of organosilicon compounds I. The migratory aptitudes of various organic groups in the aluminum chloride-catalyzed rearrangement of (chloromethyl)triorganosilanes
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference33 articles.
1. Intramolecular Rearrangement of Chloromethyltrimethylsilane1
2. New Intramolecular Rearrangements of α-Chloroalkysilicon Compounds1,2
3. Synthesis and Intramolecular Rearrangements of Chloromethylpenta-methyldisilane and 1-Chloromethyl-2-chlorotetramethyldisilane
4. The synthesis and reactions of certain disilanes containing chloromethyl groups
5. Organosilicon compounds XXXIV. The rearrangement of aryldimethyl(chloromethyl)-silanes catalysed by aluminium chloride. With a note on siliconium ions
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1. Synthesis of bulky tris[(dimethyl(alkyl/aryl)silyl)methyl]stannanes as radical based reducing agents;Journal of Organometallic Chemistry;2011-09
2. The synthesis of chlorosilanes from alkoxysilanes, silanols, and hydrosilanes with bulky substituents;Journal of Organometallic Chemistry;2006-01
3. Aluminum Chloride-Catalyzed Intramolecular Allyl-Migration Reaction of Allyl(chloromethyl)silanes and Trapping of the Intermediate with Allyltrimethylsilane;Organometallics;2004-08-27
4. Synthesis and thermal stability of silicon-containing esters of phosphorus acids;Russian Chemical Bulletin;1998-09
5. Unimolecular rearrangement of α-silylcarbenium ions. An ab initio study;Journal of Organometallic Chemistry;1996-03
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