Bi(OTf)3 Catalyzed Solvent Free Approach to Unsymmetrical Diaryl(2‐indolyl)methanes through 1,6‐Conjugate Addition of 3‐Substituted Indoles to para‐Quinone Methides

dc.contributor.authorGoswami, P.
dc.contributor.authorAnand, R.V.
dc.date.accessioned2020-12-03T04:22:20Z
dc.date.available2020-12-03T04:22:20Z
dc.date.issued2016
dc.description.abstractAn efficient 1,6‐conjugate addition of 3‐substituted indoles to para‐quinone methides (p‐QMs) using catalytic amount of Bi(OTf)3 is described. This mild and atom‐economical protocol allowed us to access unsymmetrical diaryl(2‐indolyl)methanes in moderate to excellent yields under solvent‐free grinding conditions.en_US
dc.identifier.citationChemistrySelect, 1(10), pp. 2556-2559en_US
dc.identifier.otherhttps://doi.org/10.1002/slct.201600553
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/slct.201600553
dc.identifier.urihttp://hdl.handle.net/123456789/2536
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.subjectIndolesen_US
dc.subjectDiarylindolylmethanesen_US
dc.subject1,6-conjugate additionen_US
dc.subjectSolvent free reactionen_US
dc.subjectAtom economyen_US
dc.titleBi(OTf)3 Catalyzed Solvent Free Approach to Unsymmetrical Diaryl(2‐indolyl)methanes through 1,6‐Conjugate Addition of 3‐Substituted Indoles to para‐Quinone Methidesen_US
dc.typeArticleen_US

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