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Copper‐Catalyzed Reductive Cross‐Coupling of Nonactivated Alkyl Tosylates and Mesylates with Alkyl and Aryl Bromides
116
Citations
43
References
2014
Year
Benzochromene DerivativesChemical EngineeringNonactivated Alkyl TosylatesCopper‐catalyzed Reductive Cross‐couplingEngineeringCross-coupling ReactionNatural SciencesDiversity-oriented SynthesisAvailable SubstratesOrganic ChemistryOrganometallic CatalysisCatalysisStereoselective SynthesisChemistryAsymmetric CatalysisBiomolecular EngineeringAryl Bromides
A copper-catalyzed reductive cross-coupling reaction of nonactivated alkyl tosylates and mesylates with alkyl and aryl bromides was developed. It provides a practical method for efficient and cost-effective construction of aryl-alkyl and alkyl-alkyl CC bonds with stereocontrol from readily available substrates. When used in an intramolecular fashion, the reaction enables convenient access to various substituted carbo- or heterocycles, such as 2,3-dihydrobenzofuran and benzochromene derivatives.
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