Abstract
Synthesis of the A/D/E-ring core compounds of maoecrystal V was achieved. The key Diels-Alder reactions between tricyclic αmethylene lactones and Kitahara-Danishefsky dienes afforded the spirocyclic core compounds in a regioselective and stereoselective manner.
| Original language | English |
|---|---|
| Pages (from-to) | 733-741 |
| Number of pages | 9 |
| Journal | Bioscience, Biotechnology and Biochemistry |
| Volume | 88 |
| Issue number | 7 |
| DOIs | |
| Publication status | Published - Jul 1 2024 |
Keywords
- Diels-Alder reaction
- intramolecular aldol reaction
- maoecrystal V
- synthesis
ASJC Scopus subject areas
- Analytical Chemistry
- Biotechnology
- Biochemistry
- Applied Microbiology and Biotechnology
- Molecular Biology
- Organic Chemistry
Fingerprint
Dive into the research topics of 'Synthesis of the A/D/E-ring Core Compounds of Maoecrystal V'. Together they form a unique fingerprint.Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS