The Wittig-cyclization procedure
| dc.contributor.author | Ay, K | |
| dc.contributor.author | Çetin, F | |
| dc.contributor.author | Yüceer, L | |
| dc.date.accessioned | 2024-07-18T12:00:58Z | |
| dc.date.available | 2024-07-18T12:00:58Z | |
| 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 ringclosures took place in one pot reactions. (c) 2007 Elsevier Ltd. All rights reserved. | |
| dc.identifier.issn | 0008-6215 | |
| dc.identifier.other | 1873-426X | |
| dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/8075 | |
| dc.language.iso | English | |
| dc.publisher | ELSEVIER SCI LTD | |
| dc.subject | C-GLYCOSYL COMPOUNDS | |
| dc.subject | STEREOSELECTIVITY | |
| dc.subject | CHEMISTRY | |
| dc.subject | LACTONES | |
| dc.title | The Wittig-cyclization procedure | |
| dc.type | Article |