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Total synthesis and biological evaluation of verticipyrone and analogues
- Source :
- Organic letters. 9(1)
- Publication Year :
- 2006
-
Abstract
- [reaction: see text] Total synthesis of verticipyrone, a novel NADH-fumarate reductase inhibitor, has been accomplished by a convergent approach using novel "Reverse Julia olefination" method. During total synthetic studies, we also prepared and evaluated several synthetic verticipyrone analogues, some of which exhibited more potent antiparasitic activity than the natural verticipyrone.
- Subjects :
- Aldehydes
Oxidoreductases Acting on CH-CH Group Donors
Julia olefination
Molecular Structure
Antiparasitic
medicine.drug_class
Chemistry
Organic Chemistry
Total synthesis
Verticipyrone
Reductase
Alkenes
Biochemistry
Combinatorial chemistry
Structure-Activity Relationship
Pyrones
medicine
Organic chemistry
Physical and Theoretical Chemistry
Biological evaluation
Subjects
Details
- ISSN :
- 15237060
- Volume :
- 9
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Organic letters
- Accession number :
- edsair.doi.dedup.....c71c0363bebaf6b93b75358989945412