<scp>Palladium‐Catalyzed Long‐Range</scp> Isomerization of Aryl Olefins-Reference-Cited by-同舟云学术

Palladium‐Catalyzed Long‐Range Isomerization of Aryl Olefins

Published:2022-07-18 Issue:19 Volume:40 Page:2269-2275
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Ge Qianyi¹,Meng Jingjie²,Liu Huikang²,Yang Zehua¹,Wu Zhengxing²,Zhang Wanbin²

Affiliation:

1. Hunan Provincial Key Laboratory of Tumor Microenvironment Responsive Drug Research, Institute of Pharmacy & Pharmacology School of Pharmaceutical Science, Hengyang Medical School University of South China Hengyang Hunan 421001 China

2. Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Frontiers Science Center for Transformative Molecules School of Chemistry and Chemical Engineering Shanghai Jiao Tong University, 800 Dongchuan Road Shanghai 200240 China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202200254

Reference84 articles.

1. For reviews on double‐bond isomerization see: (a) Uma R.; Crévisy C.; Grée R. Transposition of Allylic Alcohols into Carbonyl Compounds Mediated by Transition Metal Complexes.Chem. Rev.2003 103 27–52;

2. Transition metal complexes as catalysts of double-bond migration in O-allyl systems

3. Double bond migration in N-allylic systems catalyzed by transition metal complexes

4. Catalytic Isomerization of Allylic Alcohols in Water

5. Well-defined transition metal hydrides in catalytic isomerizations

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