N-Heterocyclic Carbene Catalyzed Highly Chemoselective Intermolecular Crossed Acyloin Condensation of Aromatic Aldehydes with Trifluoroacetaldehyde Ethyl Hemiacetal

dc.contributor.authorRamanjaneyulu, B.T.
dc.contributor.authorMahesh, S.
dc.contributor.authorAnand, R.V.
dc.date.accessioned2020-12-11T06:13:17Z
dc.date.available2020-12-11T06:13:17Z
dc.date.issued2015
dc.description.abstractA highly chemoselective intermolecular crossed acyloin condensation between aromatic aldehydes and trifluoroacetaldehyde ethyl hemiacetal has been developed under mild reaction conditions using N-heterocyclic carbene as a catalyst. A wide range of aromatic aldehydes bearing electron-withdrawing and -donating substituents underwent a smooth transformation to their corresponding trifluoromethyl containing acyloin derivatives in moderate to good yields.en_US
dc.identifier.citationOrganic Letters, 17 (1) pp. 6-9en_US
dc.identifier.other10.1021/ol502581b
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/ol502581b
dc.identifier.urihttp://hdl.handle.net/123456789/3023
dc.language.isoen_USen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectAldehydesen_US
dc.subjectCondensationen_US
dc.subjectCatalystsen_US
dc.subjectChemical reactionsen_US
dc.titleN-Heterocyclic Carbene Catalyzed Highly Chemoselective Intermolecular Crossed Acyloin Condensation of Aromatic Aldehydes with Trifluoroacetaldehyde Ethyl Hemiacetalen_US
dc.typeArticleen_US

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