General Synthesis of <i>N</i>-CF<sub>3</sub> Heteroaryl Amides via Successive Fluorination and Acylation of Sterically Hindered Isothiocyanates-Reference-Cited by-同舟云学术

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General Synthesis of N-CF₃ Heteroaryl Amides via Successive Fluorination and Acylation of Sterically Hindered Isothiocyanates

Published:2023-10-12 Issue:21 Volume:88 Page:15237-15248
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Tao Min¹,Qian Jiasheng¹,Chen Zuanguang¹^ORCID,An Lin-Kun¹^ORCID,Wilson David M.²^ORCID,Liu Jianbo³^ORCID

Affiliation:

1. School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, Guangdong, China

2. Department of Radiology and Biomedical Imaging, University of California, San Francisco, San Francisco, California 94158, United States

3. Department of Nuclear Medicine, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, Guangdong, China

Funder

Sun Yat-sen University

National Institute of Biomedical Imaging and Bioengineering

National Natural Science Foundation of China

Guangdong High-level Talents Program

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c01740

Reference35 articles.

1. Rethinking amide bond synthesis

2. Physicochemical Descriptors of Aromatic Character and Their Use in Drug Discovery

3. Tuberculosis: An Overview of the Immunogenic Response, Disease Progression, and Medicinal Chemistry Efforts in the Last Decade toward the Development of Potential Drugs for Extensively Drug-Resistant Tuberculosis Strains

4. Allosteric modulation of G protein‐coupled receptors by amiloride and its derivatives. Perspectives for drug discovery?

5. A Review of Current Knowledge of Resistance Aspects for the Next-Generation Succinate Dehydrogenase Inhibitor Fungicides

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