The Wittig-cyclization procedure: acid promoted intramolecular formation of 3-C-branched-chain 3,6-anhydro furano sugars via 2′-oxopropylene derivatives
| dc.contributor.author | Ay K. | |
| dc.contributor.author | Çetin F. | |
| dc.contributor.author | Yüceer L. | |
| dc.date.accessioned | 2025-04-10T11:16:43Z | |
| dc.date.available | 2025-04-10T11:16:43Z | |
| dc.date.issued | 2007 | |
| dc.description.abstract | Some olefinic Wittig products, 3-deoxy-5,6-O-isopropylidene-3-C-(2′-oxopropylene)-1,2-O-alkylidene hexofuranose derivatives were converted to the branched-chain 3,6-anhydro-3-C-(2′-oxopropyl) derivatives on treatment with ion exchange resin Amberlite 120 (H+) in methanol-water at room temperature. Hydrolysis of 5,6-isopropylidene groups and intramolecular ring-closures took place in one pot reactions. © 2007 Elsevier Ltd. All rights reserved. | |
| dc.identifier.DOI-ID | 10.1016/j.carres.2007.02.021 | |
| dc.identifier.uri | http://hdl.handle.net/20.500.14701/52015 | |
| dc.title | The Wittig-cyclization procedure: acid promoted intramolecular formation of 3-C-branched-chain 3,6-anhydro furano sugars via 2′-oxopropylene derivatives | |
| dc.type | Article |