Journal
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2012, Issue 17, Pages 3237-3248Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201200210
Keywords
Synthetic methods; Natural products; Enzymes; Inhibitors; Phosphorus; Palladium; Arylation
Categories
Funding
- Bayer Crop-Science
- Agence Nationale de la Recherche et de la Technologie (ANRT)
Ask authors/readers for more resources
Fosmidomycin (1a) and FR-90098 are potent inhibitors of 1-deoxy-D-xylulose-5-phosphate reductoisomerase (DXR), the second enzyme of the non-mevalonate (MEP) pathway responsible for the biosynthesis of isoprenoids. This paper describes the synthesis of four types of targets bearing a phosphanyl-phosphonic acid motif as the common core for the inhibition of DXR. In these structures, the hydroxamic acid was replaced by various chelators based on a phosphinic acid linked to different functional groups capable of forming five- or six-membered chelating rings.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available