Asymmetric Total Synthesis of Natural Lindenane Sesquiterpenoid Oligomers via a Triene as a Potential Biosynthetic Intermediate-Reference-Cited by-同舟云学术

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Asymmetric Total Synthesis of Natural Lindenane Sesquiterpenoid Oligomers via a Triene as a Potential Biosynthetic Intermediate

Published:2022-06 Issue:29 Volume:61 Page:
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew Chem Int Ed

Author:

Huang Zhengsong¹,Huang Ganxing¹,Wang Xiao¹,Qin Song¹,Fu Shaomin¹,Liu Bo¹^ORCID

Affiliation:

1. College of Chemistry Sichuan University 29 Wangjiang Rd. Chengdu Sichuan 610064 China

Funder

Department of Science and Technology of Sichuan Province

National Natural Science Foundation of China

Sichuan University

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.202204303

Reference72 articles.

1. Sesquiterpene dimer and trimer from Chloranthus japonicus

2. Symmetric sesquiterpene dimer from Chloranthus serratus

3. Nine sesquiterpenoid dimers with four unprecedented types of carbon skeleton from Chloranthus henryi var. hupehensis

4.

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3. A Photoinduced Radical Cascade Cyclization for the Synthesis of Angularly Fused Tricyclic Compounds;Organic Letters;2024-05-28

4. Trisarcglaboids A and B, two cytotoxic lindenane sesquiterpenoid trimers with a unique polymerization mode isolated from Sarcandra glabra;Bioorganic Chemistry;2024-05

5. Terpenoids of plants from Chloranthaceae family: chemistry, bioactivity, and synthesis;Natural Product Reports;2024

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