Tandem geminal dialkylation: Nucleophilic double addition of organocopper reagents to 3-ethynyl-2-cycloalkenones

Sang Ho Lee, Martin Hulce

Research output: Contribution to journalArticle

10 Scopus citations

Abstract

Enynones 1 undergo regiospecific double addition of organocopper reagents at their terminal sp-hybridized carbons to yield enones 2 or 3.

Original languageEnglish (US)
Pages (from-to)311-314
Number of pages4
JournalTetrahedron Letters
Volume31
Issue number3
DOIs
StatePublished - 1990
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Tandem geminal dialkylation: Nucleophilic double addition of organocopper reagents to 3-ethynyl-2-cycloalkenones'. Together they form a unique fingerprint.

  • Cite this