Syntheses of Skeletally Diverse Tetracyclic Isodon Diterpenoid Scaffolds Guided by Dienyne Radical Cyclization Logic-Reference-Cited by-同舟云学术

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Syntheses of Skeletally Diverse Tetracyclic Isodon Diterpenoid Scaffolds Guided by Dienyne Radical Cyclization Logic

Published:2020-10-06 Issue:20 Volume:22 Page:7991-7996
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Weilong,Yue Zongwei,Wang Zhen,Li Houhua,Lei Xiaoguang^ORCID

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Beijing Outstanding Young Scientist Program

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c02920

Reference67 articles.

1. Diterpenoids from Isodon species and their biological activities

2. Diterpenoids from Isodon species: an update

3. Diterpenoids of terrestrial origin

4. The Total Synthesis ofIsodonDiterpenes

5. Constructive innovation of approaching bicyclo[3.2.1]octane in ent-kauranoids

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1. Synthetic Studies toward Pseudolaric Acids: Radical Cyclization to Form Bridged Scaffold;Chinese Journal of Chemistry;2024-03-19

2. 5-epi-ent-Kaurane diterpenoids from the aerial parts of Isodon eriocalyx and their anti-atherosclerotic potential;Phytochemistry;2023-05

3. Asymmetric Synthesis of AB Rings in ent-Kaurene Carbon Framework;Chinese Journal of Organic Chemistry;2022

4. (−)‐Isoscopariusin A, a Naturally Occurring Immunosuppressive Meroditerpenoid: Structure Elucidation and Scalable Chemical Synthesis;Angewandte Chemie International Edition;2021-03-30

5. (−)‐Isoscopariusin A, a Naturally Occurring Immunosuppressive Meroditerpenoid: Structure Elucidation and Scalable Chemical Synthesis;Angewandte Chemie;2021-03-30

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