A vinylsilane route to trans-7a-methylhydrind-4-en-1,6-dione

Scott E. Denmark, Juris P. Germanas

Research output: Contribution to journalArticle

Abstract

A stereoselective synthesis of the title compound is described. The overall yield is 34% starting with 2-methyl-2-cyclopentenone. The trans ring-fusion stereochemistry is established by a conjugate addition/trapping sequence.

Original languageEnglish (US)
Pages (from-to)1231-1234
Number of pages4
JournalTetrahedron Letters
Volume25
Issue number12
DOIs
StatePublished - 1984

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Stereochemistry
Fusion reactions
vinylsilane
cyclopentenone

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

A vinylsilane route to trans-7a-methylhydrind-4-en-1,6-dione. / Denmark, Scott E.; Germanas, Juris P.

In: Tetrahedron Letters, Vol. 25, No. 12, 1984, p. 1231-1234.

Research output: Contribution to journalArticle

Denmark, Scott E. ; Germanas, Juris P. / A vinylsilane route to trans-7a-methylhydrind-4-en-1,6-dione. In: Tetrahedron Letters. 1984 ; Vol. 25, No. 12. pp. 1231-1234.
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