Elimination–rearrangement in β-functionalised silanes—the direction of the rearrangement and its scope
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1992/P2/P29920000741
Reference4 articles.
1. Protophilic versus silicophilic reactions in β-substituted silanes
2. Carbon acids. 13. Acidifying effects of phenylthio substituents
3. Acidities of carbon acids. IV. Kinetic vs. equilibrium acidities as measures of carbanion stabilities. Relative effects of phenylthio, diphenylphosphino, and phenyl groups
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2. Carbanionic Rearrangements of Halomethylenecyclobutanes. Stereochemistry of the Migrating Group;The Journal of Organic Chemistry;2010-10-06
3. ChemInform Abstract: Elimination-Rearrangement in β-Functionalized Silanes - The Direction of the Rearrangement and Its Scope.;ChemInform;2010-08-21
4. Phenyl group acceleration of [1,4] carbon-to-oxygen silicon-mediated elimination–rearrangement in β-silyl sulfones. Synthesis of O-silylated cinnamyl alcoholsDedicated to Professor Giuseppe Capozzi on the occasion of his 60th birthday.;Journal of the Chemical Society, Perkin Transactions 1;2001-12-04
5. Desulfonylation reactions: Recent developments;Tetrahedron;1999-08
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