Homochiral ketals in organic synthesis. Enantioselective synthesis of [m.n.1] Propellanones

Eugene A Mash, Keith A. Nelson

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

Optically active [m.n.1]propellanones have been prepared by diastereoselective cyclopropanation of homochiral one ketals derived from 1,4-di-O-benzyl-L-threitol and readily available bicyclic enones.

Original languageEnglish (US)
Pages (from-to)1441-1444
Number of pages4
JournalTetrahedron Letters
Volume27
Issue number13
DOIs
StatePublished - 1986

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Synthetic Chemistry Techniques
threitol

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Homochiral ketals in organic synthesis. Enantioselective synthesis of [m.n.1] Propellanones. / Mash, Eugene A; Nelson, Keith A.

In: Tetrahedron Letters, Vol. 27, No. 13, 1986, p. 1441-1444.

Research output: Contribution to journalArticle

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