Effects of varying the media for base cleavage of some Benzyl-silicon and -tin compounds in alcohols
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference18 articles.
1. Organosilicon compounds. Part XI. The alkali-catalysed cleavage of substitute benzyltrimethylsilanes
2. Organosilicon compounds XXXIII. Additional substituent effects in alkali cleavage of benzyltrimethylsilanes
3. Organosilicon compounds. Part LIII. Base cleavage of substituted fluoren-9-yltrimethylsilanes and related compounds
4. 433. Alkali-cleavage of some carbon–silicon, –germanium, and –tin bonds
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2. Cross‐Electrophile Coupling of Vinyl Halides with Alkyl Halides;Chemistry – A European Journal;2016-04-28
3. Cleavage of 5-nitro-2-(trimethylsilylmethyl)thiophene by methanolic sodium methoxide. U.v. spectroscopic and solvent isotope effect evidence for generation of the anion [5-O2N·C4H2S· CH2-2]–;J. Chem. Soc., Chem. Commun.;1985
4. Base cleavage of R–SiMen(OMe)3 –nbonds (R =m-ClC6H4CH2, PhCC, or Cl2CH) and alkoxy exchange in RSiMen(OMe)3 –n(R =m-ClC6H4CH2);J. Chem. Soc., Perkin Trans. 2;1985
5. Base cleavage of R–Si bonds of silanols RSiMe2OH. A proposed new mechanism of substitution at silicon;J. Chem. Soc., Perkin Trans. 2;1984
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