Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone.

Gary H. Posner, Timothy P. Kogan, Martin Hulce

Research output: Contribution to journalArticle

76 Citations (Scopus)

Abstract

Asymmetric synthetic methodology is introduced for preparation of 3,3-disubstituted cyclopentanones, including (+)-α-cuparenone, of high enantiomeric purity.

Original languageEnglish
Pages (from-to)383-386
Number of pages4
JournalTetrahedron Letters
Volume25
Issue number4
DOIs
StatePublished - 1984
Externally publishedYes

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Carbon
alpha-cuparenone
cyclopentanone

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone. / Posner, Gary H.; Kogan, Timothy P.; Hulce, Martin.

In: Tetrahedron Letters, Vol. 25, No. 4, 1984, p. 383-386.

Research output: Contribution to journalArticle

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