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Enantioselective Conjugate Addition of Alkenylboronic Acids to Indole-Appended Enones
75
Citations
76
References
2011
Year
Alkynylboronic EstersUnprotected Indole-appended EnonesDerivativesEngineeringNatural SciencesDiversity-oriented SynthesisAlkenylboronic AcidsOrganic ChemistryCatalysisStereoselective SynthesisChemistryNatural Product SynthesisAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
An enantioselective addition of alkenylboronic acids and alkynylboronic esters to unprotected indole-appended enones is reported. This transformation proceeds with high enantioselectivity and high product yields via the use of catalytic amounts of 3,3′-bis(pentafluorophenyl)-BINOL and Mg(Ot-Bu)2. A range of α-branched indole derivatives are available from the transformation.
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