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Palladium-Catalyzed Reaction of <i>o</i>-Alkynyltrifluoroacetanilides with 1-Bromoalkynes. An Approach to 2-Substituted 3-Alkynylindoles and 2-Substituted 3-Acylindoles
108
Citations
18
References
2005
Year
Cross-coupling ReactionEnantioselective SynthesisEngineeringAlkene MetathesisOrganic ChemistryCatalysisChemistryAsymmetric Catalysis2-Substituted 3-AcylindolesOne-pot Cyclization-hydration Protocol2-Substituted 3-AlkynylindolesPalladium-catalyzed Reaction
The palladium-catalyzed reaction of o-alkynyltrifluoroacetanilides with 1-bromoalkynes affords free N-H 2-substituted 3-alkynylindoles in satisfactory to high yield. 2-Substituted 3-alkynylindoles revealed useful intermediates for the regioselective synthesis of 2-substituted 3-acylindoles. The latter can be prepared from o-alkynyltrifluoroacetanilides and 1-bromoalkynes via a one-pot cyclization-hydration protocol, omitting the isolation of 2-substituted 3-alkynylindoles.
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