| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5212813 | Tetrahedron | 2017 | 9 Pages |
Abstract
Fifteen new adducts of acylphloroglucinol and monoterpene (α-phellandrene) featured a 2,3-dihydrobenzofuran core were isolated from the fruits of Callistemon viminalis. An oxidative [3+2] cycloaddition between acylphloroglucinol and monoterpene was speculated as the key step in the biosynthetic pathway.192
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lin Wu, Ya-Long Zhang, Xiao-Bing Wang, Yang-Mei Zhang, Ming-Hua Yang, Jun Luo, Ling-Yi Kong,
![First Page Preview: Viminalins A-O: Diverse [3+2] hybrids of acylphloroglucinol and α-phellandrene from the fruits of Callistemon viminalis Viminalins A-O: Diverse [3+2] hybrids of acylphloroglucinol and α-phellandrene from the fruits of Callistemon viminalis](/preview/png/5212813.png)