Melipatulinones A–C, Three Lignan–Phloroglucinol Hybrids from Melicope patulinervia
Author:
Affiliation:
1. Jiangsu Key Laboratory of Bioactive Natural Product Research and State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, People’s Republic of China
Funder
Ministry of Education of the People's Republic of China
Ministry of Science and Technology of the People's Republic 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.9b04680
Reference21 articles.
1. Recent advances in research on lignans and neolignans
2. Advances in the Synthesis of Lignan Natural Products
3. Stereoselective Synthesis of Tetrahydrofuran Lignans via BF3·OEt2-Promoted Reductive Deoxygenation/Epimerization of Cyclic Hemiketal: Synthesis of (−)-Odoratisol C, (−)-Futokadsurin A, (−)-Veraguensin, (+)-Fragransin A2, (+)-Galbelgin, and (+)-Talaumidin
4. Enantioselective Synthesis of the Tetrahydrofuran Lignans (–)- and (+)-Magnolone
5. Configuration and stability of naturally occurring all-cis-tetrahydrofuran lignans from Piper solmsianum
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