Modular Synthesis of Drimane Meroterpenoids Leveraging Decarboxylative Borylation and Suzuki Coupling-Reference-Cited by-同舟云学术

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Modular Synthesis of Drimane Meroterpenoids Leveraging Decarboxylative Borylation and Suzuki Coupling

Published:2020-10-27 Issue:21 Volume:22 Page:8702-8707
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wang Xia¹²,Zhang Shasha¹,Cui Pengcheng¹,Li Shengkun¹²^ORCID

Affiliation:

1. College of Plant Protection, State & Local Joint Engineering Research Center of Green Pesticide Invention and Application, Nanjing Agricultural University, Nanjing 210095, China

2. Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Guizhou University, Huaxi District, Guiyang 550025, China

Funder

State Administration of Foreign Experts Affairs

Ministry of Education of the People's Republic of China

Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c03294

Reference40 articles.

1. Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019

2. Charting biologically relevant chemical space: A structural classification of natural products (SCONP)

3. Drimane-Related Merosesquiterpenoids, a Promising Library of Metabolites for Drug Development

4. Quinone/Hydroquinone Sesquiterpenes

5. Wiedendiol-A and -B, cholesteryl ester transfer protein inhibitors from the marine sponge Xestospongia wiedenmayeri

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