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A Highly Regio- and Stereoselective Carbocupration of Fluoroalkylated Internal Alkynes: A Short Total Synthesis of the Antiestrogenic Drug Panomifene
81
Citations
8
References
2004
Year
Medicinal ChemistryAntiestrogenic Drug PanomifeneNatural SciencesMedicineDiversity-oriented SynthesisHighly Regio-Fluorous SynthesisOrganic ChemistryOrganocopper ReagentsStereoselective SynthesisChemistryShort Total SynthesisPharmacologyPharmaceutical ChemistrySynthetic ChemistryEnantioselective SynthesisDrug DiscoveryFluoroalkylated Internal Alkynes
[reaction: see text] A highly regio- and stereoselective carbometalation reaction of fluoroalkylated internal alkynes with organocopper reagents is described. This reaction is utilized successfully in the short, stereoselective total synthesis of the antiestrogenic drug panomifene.
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