Palladium-catalyzed rearrangement of silanes containing oxygen or halogen α to silicon

Vladimir Gevorgyan, Larisa Borisova, Edmunds Lukevies

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Rearrangements of tetrahydrofuryl- and tetrahydropyranyl-hydrosilanes to oxasilaalkanes, of acetoxymethyl-hydrosilanes to acetoxysilanes, and halogenomethyl-hydrosilanes to halogenosilanes in the presence of palladium catalyst have been studied. The reaction has been shown to proceed more rapidly in tetrahydrofuran and hexane than in benzene or acetonitrile. The progressive replacement of the methyl groups on the silicon atom by phenyl groups slowed down the rearrangement, as did change from five-membered to six-membered heterocycles.

Original languageEnglish (US)
Pages (from-to)277-285
Number of pages9
JournalJournal of Organometallic Chemistry
Volume436
Issue number3
DOIs
StatePublished - Sep 22 1992
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry
  • Materials Chemistry

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