Palladium‐Catalyzed Asymmetric Intramolecular Reductive Heck Desymmetrization of Cyclopentenes: Access to Chiral Bicyclo[3.2.1]octanes-Reference-Cited by-同舟云学术

Palladium‐Catalyzed Asymmetric Intramolecular Reductive Heck Desymmetrization of Cyclopentenes: Access to Chiral Bicyclo[3.2.1]octanes

Published:2019-02-25 Issue:9 Volume:131 Page:2910-2914
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Yuan Zhenbo¹,Feng Ziwen¹,Zeng Yuye¹,Zhao Xiaobin¹,Lin Aijun¹^ORCID,Yao Hequan¹^ORCID

Affiliation:

1. State Key Laboratory of Natural Medicines (SKLNM) and Jiangsu Key Laboratory of Bioactive Natural Product ResearchDepartment of Medicinal ChemistryChina Pharmaceutical University Nanjing 210009 P. R. China

Funder

the National Natural Science Foundation of China

the Innovation Team of "the Double-First Class" Disciplines

the Foundation of The Open Project of State Key Laboratory of Natural Medicines

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201900059

Reference62 articles.

1. Palladium-catalyzed conjugate addition reaction of aryl iodides with .alpha.,.beta.-unsaturated ketones

2. For selected reviews on reductive Heck reactions see:

3. The palladium-catalyzed hydroarylation and hydrovinylation of carbon-carbon multiple bonds: New perspectives in organic synthesis

4. The Heck Reaction as a Sharpening Stone of Palladium Catalysis

5. The Hydroarylation Reaction—Scope and Limitations

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