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

Journal article

Peer reviewed

Sang Ho Lee and Martin Hulce

Tetrahedron Letters, Vol.31(3), pp.311-314

1990

Abstract

Biochemistry

Drug Discovery

Organic Chemistry

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

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Title: Tandem geminal dialkylation
Creators: Sang Ho Lee (Author) - University of Maryland, Baltimore County
Martin Hulce (Author) - University of Maryland, Baltimore County
Publication Details: Tetrahedron Letters, Vol.31(3), pp.311-314
Series: 31
Number of pages: 4
Identifiers: 991005928599902656
Academic Unit: Creighton University
Language: English
Resource Type: Journal article