Inubritantrimers A–D: Trimerized Sesquiterpenoid [4 + 2] Adducts Featuring a Distinctive Spiro-Polycyclic Scaffold from <i>Inula britannica</i>-Reference-Cited by-同舟云学术

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Inubritantrimers A–D: Trimerized Sesquiterpenoid [4 + 2] Adducts Featuring a Distinctive Spiro-Polycyclic Scaffold from Inula britannica

Published:2024-03-26 Issue:7 Volume:89 Page:5029-5037
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Guo Cong¹,Qi Ruo-Yu¹,Ren Jie-Yi¹,Xu Dan-Dan²,Zhang Qiang¹^ORCID,Gao Jin-Ming¹^ORCID,Tang Jiang-Jiang¹³^ORCID

Affiliation:

1. Shaanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, No. 3 Taicheng Road, Yangling, Shaanxi, 712100, China

2. School of Foundational Education, Xizang Agricultural and Animal Husbandry University, No. 100 Yucai West Road, Nyingchi, Xizang, 860000, China

3. Shenzhen Research Institute, Northwest A&F University, Shenzhen Virtual University Park Building, High-Tech Industrial Park, Shenzhen, Guangdong, 518000, China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00248

Reference30 articles.

1. Recent Advances in Natural Product Synthesis by Using Intramolecular Diels−Alder Reactions

2. Natural [4 + 2]-Cyclases

3. Biomimetic Synthesis of Lavandiolides H, I, and K and Artematrolide F via Diels–Alder Reaction

4. Screening and identification of neuroprotective compounds relevant to Alzheimer׳s disease from medicinal plants of S. Tomé e Príncipe

5. Inulasesquiterpenoids: structural diversity, cytotoxicity and anti-tumor activity

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