Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4844
Title: Access to Hetero-Benzyl Scaffolds via Transient-Ligand-Enabled Direct gamma-C(sp(3))-H Arylation of 3-Methylheteroarene-2-Carbaldehydes
Authors: REDDY, CHENNAKESAVA
SHAIKH, JAVED Y.
BHAT, RAMAKRISHNA G.
Dept. of Chemistry
Keywords: C-H Arylation
C(SP(3))-H Bonds
Functionalization
Benzaldehydes
Alkenes
Ketone
TOC-JUN-2020
2020
2020-JUN-WEEK4
Issue Date: Apr-2020
Publisher: American Chemical Society
Citation: Journal of Organic Chemistry, 85(11), 6924-6934.
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.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/4844
https://doi.org/10.1021/acs.joc.0c00154
ISSN: 0022-3263
1520-6904
Appears in Collections:JOURNAL ARTICLES

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