Regio- and Enantioselective Hydromethylation of 3-Pyrrolines and Glycals Enabled by Cobalt Catalysis-Reference-Cited by-同舟云学术

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Regio- and Enantioselective Hydromethylation of 3-Pyrrolines and Glycals Enabled by Cobalt Catalysis

Published:2024-06-11 Issue:6 Volume:4 Page:2312-2322
ISSN:2691-3704
Container-title:JACS Au
language:en
Short-container-title:JACS Au

Author:

Shen Mengyang¹,Niu Caoyue¹,Wang Xuchao¹,Huang Jia-Bo²,Zhao Zhen¹,Ni Shao-Fei²^ORCID,Rong Zi-Qiang¹^ORCID

Affiliation:

1. Frontiers Science Center for Flexible Electronics (FSCFE), Shaanxi Institute of Flexible Electronics (SIFE) & Shaanxi Institute of Biomedical Materials and Engineering (SIBME), Northwestern Polytechnical University (NPU), 127 West Youyi Road, Xi’an 710072, China

2. Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Shantou, Guangdong 515063, China

Funder

Natural Science Basic Research Program of Shaanxi Province

Shantou University

National Natural Science Foundation of China

Northwestern Polytechnical University

Shaanxi Fundamental Science Research Project for Chemistry and Biology

the Fundamental Research Funds for the Central Universities

Program for Young Talents of Shaanxi Province

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacsau.4c00275

Reference111 articles.

1. Synthesis and evaluation of NS5A inhibitors containing diverse heteroaromatic cores

2. 2-Aminomethylthieno[3,2- d ]pyrimidin-4(3 H )-ones bearing 3-methylpyrazole hinge binding moiety: Highly potent, selective, and time-dependent inhibitors of Cdc7 kinase

3. Discovery of an MLLT1/3 YEATS Domain Chemical Probe

4. Discovery of a Novel, Highly Potent, and Selective Thieno[3,2-d]pyrimidinone-Based Cdc7 Inhibitor with a Quinuclidine Moiety (TAK-931) as an Orally Active Investigational Antitumor Agent

5. Discovery and Characterization of Selective and Ligand-Efficient DYRK Inhibitors

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1. A General Enantioselective α-Alkyl Amino Acid Derivatives Synthesis Enabled by Cobalt-Catalyzed Reductive Addition;Journal of the American Chemical Society;2024-09-12

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