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 |