A Mechanism Study for Self-Cleaving Chlorotetrafluoroethylsulfinyl (−SOCF2CF2Cl)-Directed Pd(II)-Catalyzed C

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A Mechanism Study for Self-Cleaving Chlorotetrafluoroethylsulfinyl (−SOCF2CF2Cl)-Directed Pd(II)-Catalyzed C–H Activation

Published:2021-11-16 Issue:23 Volume:86 Page:16511-16517
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Shao Nan-Qi¹,Wang Dong-Hui¹²^ORCID

Affiliation:

1. Laboratory of Synthetic and Self-Assembly Chemistry for Organic Functional Molecules, Shanghai Institute of Organic Chemistry, CAS, 345 Lingling Rd., Shanghai 200032, China

2. Department of Pharmacy, Nanjing University of Chinese Medicines, 138 Xianlin Ave., Nanjing 210023, China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Chinese Academy of Sciences

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c01852

Reference24 articles.

1. Palladium- and Copper-Catalyzed Arylation of Carbon−Hydrogen Bonds

2. Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions

3. Weak Coordination as a Powerful Means for Developing Broadly Useful C–H Functionalization Reactions

4. A Simple and Versatile Amide Directing Group for C−H Functionalizations

5. An Epoxide-Mediated Deprotection Method for Acidic Amide Auxiliary

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