Mechanism and Selectivity of the Oxidative Ring Contraction of Cyclic α‐Formyl Ketones-Reference-Cited by-同舟云学术

Mechanism and Selectivity of the Oxidative Ring Contraction of Cyclic α‐Formyl Ketones

Published:2019-11-13 Issue:23 Volume:14 Page:4262-4267
ISSN:1861-4728
Container-title:Chemistry – An Asian Journal
language:en
Short-container-title:Chem. Asian J.

Author:

Xu Li‐Ping¹^ORCID,Hou Xu‐Dong¹,Wang Hui¹,Zhou Jing‐Bo²,Ma Jie¹³,Zhuo Shuping¹,Wang Qian¹

Affiliation:

1. School of Chemistry and Chemical EngineeringShandong University of Technology 266 West Xincun Road Zibo 255049 P. R. China

2. Lab of Computational Chemistry and Drug DesignState Key Laboratory of Chemical OncogenomicsPeking University Shenzhen Graduate School Shenzhen 518055 P. R. China

3. Department of ChemistryCollege of ScienceChina University of Petroleum (East China) Qingdao 266580 P. R. China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Publisher

Wiley

Subject

General Chemistry,Biochemistry,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/asia.201901263

Reference44 articles.

1. Communesins G and H, New Alkaloids from the Psychrotolerant Fungus Penicillium rivulum

3. Total Synthesis of Akuammiline Alkaloid (−)-Vincorine via Intramolecular Oxidative Coupling

4. Total Synthesis of the Monoterpenoid Indole Alkaloid (±)-Aspidophylline A

5. Total Synthesis of the Monoterpenoid Indole Alkaloid (±)-Aspidophylline A

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