Publication | Closed Access
A General Palladium‐Catalyzed Suzuki–Miyaura Coupling of Aryl Mesylates
182
Citations
42
References
2008
Year
Arylboronic AcidsCross-coupling ReactionEngineeringUnactivated Aryl MesylatesNatural SciencesDiversity-oriented SynthesisOrganic ChemistryOrganometallic CatalysisCatalysisChemistryAryl MesylatesSynthetic ChemistryBiomolecular EngineeringOther Organoboron Nucleophiles
Catalyze this! The first palladium-catalyzed Suzuki–Miyaura coupling of unactivated aryl mesylates is reported, with not only arylboronic acids, but also other organoboron nucleophiles (see picture; Z=B(OH)2, BF3K, BPin). The reaction conditions are compatible with various common functional groups (R1=alkyl, OMe, CHO, CO, CN, CO2R′, heteroaryl).
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