Abstract
An efficient and convenient synthetic route to glycosyl 1-β-phosphates has been developed using diallyl chlorophosphate as a phosphorylating agent with 4-N,N-dimethylaminopyridine under mild conditions. Diallyl-glycosyl 1-β-phosphate triesters of d-manno, l-glycero-d-manno-hepto-, d-gluco-, d-galacto-, and l-fuco-pyranose as well as lactose have been obtained by this strategy in good yields and excellent β-selectivities. Furthermore, the diallyl 6-azido-mannosyl 1-β-phosphate 2 was deprotected under mild conditions and converted into potentially clickable analogues of β-mannosyl phosphoisoprenoids I and ADP-heptose II.
Original language | English |
---|---|
Pages (from-to) | 5628-5631 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 16 |
Issue number | 21 |
DOIs | |
Publication status | Published - 7 Nov 2014 |
Fingerprint
Dive into the research topics of 'β-Stereoselective phosphorylations applied to the synthesis of ADP- and polyprenyl-β-mannopyranosides'. Together they form a unique fingerprint.Equipment
-
Physical Chemistry and characterization(PC2)
Johan Wouters (Manager) & Carmela Aprile (Manager)
Technological Platform Physical Chemistry and characterizationFacility/equipment: Technological Platform