| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5225202 | Tetrahedron | 2008 | 7 Pages |
Synthesis and elucidation of absolute stereochemistry of salaprinol (3) isolated from the root and stems of Salacia prinoides, which has been used for the treatment of diabetes in India, Sri Lanka, and Southeast Asia countries, is described. Compound 3 and its 2′-epimer, epi-salaprinol (epi-3) were synthesized via the coupling reaction of a cyclic sulfate, 2-O-benzylglycerol 1,3-cyclic sulfate (5), with a thiosugar, 1,4-dideoxy-1,4-epithio-d-arabinitol (6), as the key reaction, and S configuration of the asymmetric center in the side chain of 3 was elucidated by the X-ray crystallographic analysis.
Graphical abstractElucidation of absolute stereochemistry of salaprinol (3) isolated from Salacia prinoides, which has been used for the treatment of diabetes in India, Sri Lanka, and Southeast Asia countries, is described. Compound 3 and its 2′-epimer epi-3 were synthesized via the coupling reaction of 5 with 6 as the key reaction, and S configuration of C2′ in the side chain of 3 was elucidated by the X-ray crystallographic analysis.Figure optionsDownload full-size imageDownload as PowerPoint slide
