Asymmetric Total Synthesis of Dankasterones A and B and Periconiastone A Through Radical Cyclization-Reference-Cited by-同舟云学术

Asymmetric Total Synthesis of Dankasterones A and B and Periconiastone A Through Radical Cyclization

Published:2021-01-07 Issue:10 Volume:133 Page:5572-5578
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Chen Pengquan¹,Wang Cheng¹,Yang Rui¹,Xu Hongjin¹,Wu Jinghua¹,Jiang Huanfeng¹,Chen Kai²³,Ma Zhiqiang¹^ORCID

Affiliation:

1. Key Lab of Functional Molecular Engineering of Guangdong Province School of Chemistry & Chemical Engineering South China University of Technology Wushan Road-381 Guangzhou 510641 China

2. College of Chemistry and Chemical Engineering Central South University Changsha 410083 China

3. Lab of Computational Chemistry and Drug Design State Key Laboratory of Chemical Oncogenomics Peking University Shenzhen Graduate School Shenzhen 518055 China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.202013881

Reference117 articles.

1. For the isolation of dankasterones see:

2. Dankasterone, a new class of cytotoxic steroid produced by a Gymnascella species from a marine sponge

3. Variation in Cytostatic Constituents of a Sponge-Derived Gymnascella dankaliensis by Manipulating the Carbon Source

4. Periconiastone A, an Antibacterial Ergosterol with a Pentacyclo[8.7.0.01,5.02,14.010,15]heptadecane System from Periconia sp. TJ403-rc01

5. For selected reviews about synthesis or isolation of natural products containingcis-decalins see:

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