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Access to Hetero-Benzyl Scaffolds via Transient-Ligand-Enabled Direct gamma-C(sp(3))-H Arylation of 3-Methylheteroarene-2-Carbaldehydes

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dc.contributor.author REDDY, CHENNAKESAVA en_US
dc.contributor.author SHAIKH, JAVED Y. en_US
dc.contributor.author BHAT, RAMAKRISHNA G. en_US
dc.date.accessioned 2020-06-26T05:09:46Z
dc.date.available 2020-06-26T05:09:46Z
dc.date.issued 2020-04 en_US
dc.identifier.citation Journal of Organic Chemistry, 85(11), 6924-6934. en_US
dc.identifier.issn 0022-3263 en_US
dc.identifier.issn 1520-6904 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4844
dc.identifier.uri https://doi.org/10.1021/acs.joc.0c00154 en_US
dc.description.abstract An 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.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject C-H Arylation en_US
dc.subject C(SP(3))-H Bonds en_US
dc.subject Functionalization en_US
dc.subject Benzaldehydes en_US
dc.subject Alkenes en_US
dc.subject Ketone en_US
dc.subject TOC-JUN-2020 en_US
dc.subject 2020 en_US
dc.subject 2020-JUN-WEEK4 en_US
dc.title Access to Hetero-Benzyl Scaffolds via Transient-Ligand-Enabled Direct gamma-C(sp(3))-H Arylation of 3-Methylheteroarene-2-Carbaldehydes en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Journal of Organic Chemistry en_US
dc.publication.originofpublisher Foreign en_US


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