Pd‐Catalyzed Regio‐ and Diastereoselective Heck Cyclization to Access Bicyclo[3.2.1]octanone Ring Systems-Reference-Cited by-同舟云学术

Pd‐Catalyzed Regio‐ and Diastereoselective Heck Cyclization to Access Bicyclo[3.2.1]octanone Ring Systems

Published:2020-09-09 Issue:20 Volume:12 Page:5058-5061
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Li Bo¹,Zhang Guiming¹,Xu Tao¹²^ORCID

Affiliation:

1. Key Laboratory of Marine Drugs Ministry of Education School of Medicine and Pharmacy Ocean University of China 5 Yushan Road Qingdao 266003 P. R. China

2. Laboratory for Marine Drugs and Bioproducts & Open Studio for Druggability Research of Marine Natural Products Pilot National Laboratory for Marine Science and Technology 1 Wenhai Road Qingdao 266237 P. R. China

Funder

Fundamental Research Funds for the Central Universities

National Natural Science Foundation of China

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.202001089

Reference95 articles.

1. For selected reviews see:

2. Synthesis of Functionalized Bicyclo[3.2.1]octanes and Their Multiple Uses in Organic Chemistry

3. Syntheses and Applications of Functionalized Bicyclo[3.2.1]octanes: Thirteen Years of Progress

4. Total Synthesis of Natural Products with Bridged Bicyclo[m.n.1] Ring Systems via Type II [5 + 2] Cycloaddition

5. The synthesis of functionalized bridged polycycles via C–H bond insertion

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