Intermolecular Buchwald–Hartwig Reactions for Enantioselective Synthesis of Diverse Atropisomers: Rerouting the C–N Forming Mechanism to Substrate Oxygen-Assisted Reductive Elimination-Reference-Cited by-同舟云学术

Intermolecular Buchwald–Hartwig Reactions for Enantioselective Synthesis of Diverse Atropisomers: Rerouting the C–N Forming Mechanism to Substrate Oxygen-Assisted Reductive Elimination

Published:2024-06-07 Issue:24 Volume:146 Page:16567-16580
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Wang Wei¹,Jiang Mingwei¹,Li Junwei¹,Wang Fen¹,Li Xiao-Xi²^ORCID,Zhao Jing³^ORCID,Li Xingwei¹²^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi’an 710062, China

2. Institute of Frontier Chemistry, School of Chemistry and Chemical Engineering, Shandong University, Qingdao 266237, China

3. School of Chemistry and Chemical Engineering and Shenzhen Research Institute, Nanjing University, Nanjing 210093, China

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

SNNU

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.4c03342

Reference111 articles.

1. New Chiral Phosphorus Ligands for Enantioselective Hydrogenation

2. The Challenge of Atropisomerism in Drug Discovery

3. Total synthesis of chiral biaryl natural products by asymmetric biaryl coupling

4. Atroposelective Total Synthesis of Axially Chiral Biaryl Natural Products

5. A twist of nature – the significance of atropisomers in biological systems

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