in situ Formation of RSCl/ArSeCl and Their Oxidative Coupling with Enaminone Derivatives Under Transition‐metal Free Conditions-Reference-Cited by-同舟云学术

in situ Formation of RSCl/ArSeCl and Their Oxidative Coupling with Enaminone Derivatives Under Transition‐metal Free Conditions

Published:2019-09-19 Issue:21 Volume:361 Page:4926-4932
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Shang Zhenhua¹,Chen Qingyu¹,Xing Linlin²,Zhang Yilin³,Wait Laura⁴,Du Yunfei²

Affiliation:

1. College of Chemical and Pharmaceutical EngineeringHebei University of Science and Technology; Hebei Research Center of Pharmaceutical and Chemical Engineering Shijiazhuang 050018 People's Republic of China

2. Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, School of Pharmaceutical Science and TechnologyTianjin University Tianjin 300072 People's Republic of China

3. C. Eugene Bennett Department of ChemistryWest Virginia University, Morgantown West Virginia 26506-6045 United States

4. School of Chemistry and Molecular BiosciencesThe University of Queensland St Lucia, Queensland 4068 Australia

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201900940

Reference76 articles.

2. Copper-catalyzed, hypervalent iodine mediated CC bond activation of enaminones for the synthesis of α-keto amides