Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4844
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dc.contributor.authorREDDY, CHENNAKESAVAen_US
dc.contributor.authorSHAIKH, JAVED Y.en_US
dc.contributor.authorBHAT, RAMAKRISHNA G.en_US
dc.date.accessioned2020-06-26T05:09:46Z-
dc.date.available2020-06-26T05:09:46Z-
dc.date.issued2020-04en_US
dc.identifier.citationJournal of Organic Chemistry, 85(11), 6924-6934.en_US
dc.identifier.issn0022-3263en_US
dc.identifier.issn1520-6904en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4844-
dc.identifier.urihttps://doi.org/10.1021/acs.joc.0c00154en_US
dc.description.abstractAn efficient and straightforward method has been developed for the synthesis of β-benzyl-substituted 5-membered heterocyclic carbaldehydes via transient directing-group-enabled direct γ-C(sp3)–H arylation of 3-methylheteroarene-2-carbaldehydes. A wide range of 3-methylheteroarene carbaldehydes undergo coupling with a variety of aryl iodides, including less reactive iodo pyridine derivatives to provide a library of highly selective functionalized products in good to excellent yields. Some of these products have been successfully utilized in synthesizing useful synthetic intermediates.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectC-H Arylationen_US
dc.subjectC(SP(3))-H Bondsen_US
dc.subjectFunctionalizationen_US
dc.subjectBenzaldehydesen_US
dc.subjectAlkenesen_US
dc.subjectKetoneen_US
dc.subjectTOC-JUN-2020en_US
dc.subject2020en_US
dc.subject2020-JUN-WEEK4en_US
dc.titleAccess to Hetero-Benzyl Scaffolds via Transient-Ligand-Enabled Direct gamma-C(sp(3))-H Arylation of 3-Methylheteroarene-2-Carbaldehydesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleJournal of Organic Chemistryen_US
dc.publication.originofpublisherForeignen_US
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