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

被引：0

作者：

Wang, Wei ^{[1
]}

Jiang, Mingwei ^{[1
]}

Li, Junwei ^{[1
]}

Wang, Fen ^{[1
]}

Li, Xiao-Xi ^{[2
]}

Zhao, Jing ^{[3
]}

Li, Xingwei ^{[1
,2
]}

机构：

[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

来源：

Journal of the American Chemical Society | 1600年 / 146卷 / 24期

关键词：

Financial support from the National Key R&D Program of China (no. 2022YFA1503104); the National Natural Science Foundation of China (no. 22371175); and research fund from the SNNU are gratefully acknowledged. The authors thanks Prof. Xiaolin Zhu for a graphic preparation;

D O I：

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中图分类号：

学科分类号：

摘要：

111

引用

页码：16567 / 16580

共 2 条

[1] Intermolecular Buchwald-Hartwig Reactions for Enantioselective Synthesis of Diverse Atropisomers: Rerouting the C-N Forming Mechanism to Substrate Oxygen-Assisted Reductive Elimination
Wang, Wei
Jiang, Mingwei
Li, Junwei
Wang, Fen
Li, Xiao-Xi
Zhao, Jing
Li, Xingwei
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2024, 146 (24) : 16567 - 16580
[2] 2-Phenyl-2-(4-phenyl-1H-1,2,3-triazol-1-yl)ethanol as an Efficient and Versatile Auxiliary Ligand in Copper(II)-Catalyzed Buchwald-Hartwig and Sharpless-Meldal C-N Bond-Forming Reactions
Sharghi, Hashem
Shiri, Pezhman
SYNTHESIS-STUTTGART, 2015, 47 (08): : 1131 - 1146

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