A novel approach to the tetracyclic frameworks of anislactone-type sesquiterpenoids-Reference-Cited by-同舟云学术

A novel approach to the tetracyclic frameworks of anislactone-type sesquiterpenoids

Published:2024 Issue:16 Volume:11 Page:4556-4559
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

He Long¹,Zhang Xiaocheng¹,Li Sen¹,Tian Xuexue¹,Han Yimeng¹,Xie Haitao²,Xie Weiqing¹³^ORCID

Affiliation:

1. Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, 22 Xinong Road, Yangling, 712100, Shaanxi, China

2. Department of Clinical Laboratory Medicine, Institution of Microbiology and Infectious Diseases, The First Affiliated Hospital, Heng-yang Medical School, University of South China, Hengyang, 421001, Hunan, China

3. Key Laboratory of Botanical Pesticide R&D in Shaanxi Province, Yangling, 712100, Shaanxi, China

Abstract

A novel approach for synthesizing the A-B-C-D ring system of anislactone-type sesquiterpenoids was enabled by a H2O2-mediated oxidative ring contraction reaction.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hunan Province

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO00915K

Reference27 articles.

1. Advances in the Synthesis of Anislactone-Type Sesquiterpenes

2. Merrilactone A, a novel neurotrophic sesquiterpene dilactone from Illicium merrillianum

3. Structures of merrilactones B and C, novel anislactone-type sesquiterpenes from Illicium merrillianum, and chemical conversion of anislactone B to merrilactone A

4. The Total Synthesis of (±)-Merrilactone A

5. A Synthetic Pathway to Either Enantiomer of Merrilactone A