Stereoselective Total Synthesis of Natural Decanolides Bellidisin C and Pinolidoxin
A divergent total synthesis of bioactive, naturally occurring decanolides, pinolidoxin and bellidisin C, was accomplished by taking advantage of chiral templates <i>L</i>-ribose and <i>L</i>-malic acid. In particular, bellidisin C, which is the first total synthesis so far, w...
Saved in:
| Main Authors: | Jingjing Bi, Minhao Chen, Pengpeng Nie, Yuanfang Liu, Jun Liu, Yuguo Du |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2024-11-01
|
| Series: | Molecules |
| Subjects: | |
| Online Access: | https://www.mdpi.com/1420-3049/29/23/5500 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Stereoselective strategies to access spirotetronate natural products
by: Brion, Aurélien, et al.
Published: (2024-12-01) -
Total Synthesis of Cyclosenegalin A
by: Anderson Arnold Aloanis, et al.
Published: (2024-12-01) -
Total Synthesis of Cardenolides Acospectoside A and Acovenoside B
by: Benzhang Liu, et al.
Published: (2025-05-01) -
Total Synthesis and Stereochemical Assignment of Alternapyrone
by: Hui Zhang, et al.
Published: (2025-04-01) -
Arctigenin: pharmacology, total synthesis, and progress in structure modification
by: Dan Wu, et al.
Published: (2022-12-01)