Ruthenium-Catalyzed Regioselective C(sp2)–H Activation/Annulation of N-(7-Azaindole)amides with 1,3-Diynes Using N-Amino-7-azaindole as the N,N-Bidentate Directing Group-Reference-Cited by-同舟云学术

Ruthenium-Catalyzed Regioselective C(sp2)–H Activation/Annulation of N-(7-Azaindole)amides with 1,3-Diynes Using N-Amino-7-azaindole as the N,N-Bidentate Directing Group

Published:2021-06-25 Issue:14 Volume:86 Page:9428-9443
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Pati Bedadyuti Vedvyas¹,Sagara Prateep Singh²,Ghosh Asit¹,Das Adhikari Gopal Krushna¹,Ravikumar Ponneri Chandrababu¹^ORCID

Affiliation:

1. School of Chemical Sciences, National Institute of Science Education and Research (NISER), HBNI, Bhubaneswar, Jatani, Odisha 752050, India

2. School of Basic Sciences, Indian Institute of Technology Mandi, Kamand, Himachal Pradesh 175005, India

Funder

University Grants Commission

Department of Atomic Energy, Government of India

Science and Engineering Research Board

Council for Scientific and Industrial Research

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c00759

Reference77 articles.

1. Discovery, synthesis and biological evaluation of isoquinolones as novel and highly selective JNK inhibitors (2)

2. Synthesis of isoquinolones via Rh-catalyzed C–H activation of substituted benzamides using air as the sole oxidant in water

3. Prediction of the binding mode between BMS-378806 and HIV-1 gp120 by docking and molecular dynamics simulation

4. C–H bond activation enables the rapid construction and late-stage diversification of functional molecules

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