Journal
ORGANIC LETTERS
Volume 3, Issue 21, Pages 3345-3347Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol016585z
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[GRAPHICS] Nickel-promoted alkylative or arylative carboxylation of terminal alkynes via a carbon dioxide fixation process was investigated. In the presence of a stoichiometric amount of a zero-valent nickel complex, the reaction of alkynes with CO2 gave a nickelacycle, which was reacted with various organozinc reagents under very mild conditions to provide beta,beta'-disubstituted, alpha,beta -unsaturated carboxylic acids in a highly regio- and stereoselective manner.
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