Publication | Closed Access
Zinc-Mediated Highly α-Regioselective 1,4-Addition of Chalcones with Prenyl Bromide in THF
23
Citations
52
References
2013
Year
Prenylzinc ReagentsEngineeringNatural SciencesDiversity-oriented SynthesisPrenyl BromideOrganic ChemistryOrganometallic CatalysisChemistryHeterocycle ChemistryPharmacologyReagent CombinationSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
α-Regioselective addition to chalcones was realized by use of in situ generated prenylzinc reagents from zinc and prenyl bromide in the presence of SnCl4 in a 1,4-addition fashion. The approach uses the reagent combination of prenyl bromide, zinc, and SnCl4 in THF, all of which are inexpensive, readily available, and easily removable after the reaction.
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