Sustainable Approach to Azaheterocyclic Acetamides by Decarboxylative Aminoformylation-Reference-Cited by-同舟云学术

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Sustainable Approach to Azaheterocyclic Acetamides by Decarboxylative Aminoformylation

Published:2020-09-22 Issue:44 Volume:8 Page:16463-16468
ISSN:2168-0485
Container-title:ACS Sustainable Chemistry & Engineering
language:en
Short-container-title:ACS Sustainable Chem. Eng.

Author:

Zhang Zhenxing¹^ORCID,Jia Chunqi¹,Kong Xiangtao¹,Hussain Muzammal²,Liu Zhenyu²,Liang Wanqing²,Jiang Ling³^ORCID,Jiang Hao²,Ma Junyan¹⁴⁵

Affiliation:

1. College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, P. R. China

2. Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou 510530, P. R. China

3. State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, P. R. China

4. Department of Chemistry, Clemson University, Clemson 29634, South Carolina, United States

5. Center for Optical Materials Science and Engineering Technology, Clemson 29634, South Carolina, United States

Funder

510 talent program

Henan Scientific Research Fund for Returned Scholars to Junyan

Publisher

American Chemical Society (ACS)

Subject

Renewable Energy, Sustainability and the Environment,General Chemical Engineering,Environmental Chemistry,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acssuschemeng.0c05118

Reference41 articles.

1. Anticancer and Reversing Multidrug Resistance Activities of Natural Isoquinoline Alkaloids and their Structure-activity Relationship

2. Design, Synthesis, Biochemical, and Antiviral Evaluations of C6 Benzyl and C6 Biarylmethyl Substituted 2-Hydroxylisoquinoline-1,3-diones: Dual Inhibition against HIV Reverse Transcriptase-Associated RNase H and Polymerase with Antiviral Activities

3. Lead identification to generate isoquinolinedione inhibitors of insulin-like growth factor receptor (IGF-1R) for potential use in cancer treatment

4. Specific inhibitor of puromycin-sensitive aminopeptidase with a homophthalimide skeleton: identification of the target molecule and a structure–activity relationship study

5. The design, synthesis and biological evaluations of C-6 or C-7 substituted 2-hydroxyisoquinoline-1,3-diones as inhibitors of hepatitis C virus

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