Unveiling Pre-Transmetalation Intermediates in Base-Free Suzuki–Miyaura Cross-Couplings: A Computational Study-Reference-Cited by-同舟云学术

Unveiling Pre-Transmetalation Intermediates in Base-Free Suzuki–Miyaura Cross-Couplings: A Computational Study

Published:2024-01-24 Issue:5 Volume:63 Page:2606-2615
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Xie Xiaofeng¹^ORCID,Zhang Jiejing¹,Song Xue-Qing¹^ORCID,Li Wan¹^ORCID,Cao Fei¹^ORCID,Zhou Chengyan¹^ORCID,Zhu Huajie²,Li Longfei¹^ORCID

Affiliation:

1. College of Pharmacy, Key Laboratory of Pharmaceutical Quality Control of Hebei Province, Key Laboratory of Medicinal Chemistry and Molecular Diagnosis of Ministry of Education, Hebei University, Baoding, Hebei 071002, P. R. China

2. School of Chemical and Pharmaceutical Engineering, Hebei University of Science and Technology, Shijiazhuang, Hebei 050018, P. R. China

Funder

Natural Science Foundation of Hebei Province

Hebei University

National Natural Science Foundation of China

Innovation Capacity Improvement Plan of Hebei Province

Jointed key Pharmaceutical and Drug Project of Hebei Province

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.3c03855

Reference81 articles.

1. Cross-Coupling Reactions Of Organoboranes: An Easy Way To Construct CC Bonds (Nobel Lecture)

2. Selection of boron reagents for Suzuki–Miyaura coupling

3. Factors Determining the Selection of Organic Reactions by Medicinal Chemists and the Use of These Reactions in Arrays (Small Focused Libraries)

4. Transition-metal-catalyzed Suzuki–Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts

5. Decarbonylative organoboron cross-coupling of esters by nickel catalysis