Metal-Free Addition of Alkyl Bromides to Access 3,3-Disubstituted Quinoxalinones Enabled by Visible-Light Photoredox Catalysis-Reference-Cited by-同舟云学术

Metal-Free Addition of Alkyl Bromides to Access 3,3-Disubstituted Quinoxalinones Enabled by Visible-Light Photoredox Catalysis

Published:2023-08-09 Issue:16 Volume:88 Page:11762-11766
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liao Jennie¹^ORCID,Hunter David N.²,Oloyede Ugochinyere Nancy²,McLaughlin Joseph W.²,Wang Cheng²,El Marrouni Abdellatif²^ORCID

Affiliation:

1. Process Research & Development, MRL, Merck & Co., Inc., West Point, Pennsylvania 19486, United States

2. Discovery Chemistry, MRL, Merck & Co., Inc., West Point, Pennsylvania 19486, United States

Funder

Merck

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c01054

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4. Design, synthesis, and biological evaluation of quinoxalinone derivatives as potent BRD4 inhibitors

5. aCombs, A. P.; Maduskuie, Jr, T. P.; Falahatpisheh, N. 1H-PYRROLO[2,3-C]PYRIDIN-7(6H)-ONES AND PYRAZOLO[3,4-C]PYRIDIN-7(6H)-ONES AS INHIBITORS OF BET PROTEINS. WO2015164480, 2015.

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