Chemoselective deprotection of acid labile primary hydroxyl protecting groups under CBr4-photoirradiation conditions
| dc.citation.epage | 11475 | en_US |
| dc.citation.issue | 50 | en_US |
| dc.citation.spage | 11465 | en_US |
| dc.citation.volume | 60 | en_US |
| dc.citation.woscount | 12 | |
| dc.contributor.author | Chen, MY | en_US |
| dc.contributor.author | Patkar, LN | en_US |
| dc.contributor.author | Lu, KC | en_US |
| dc.contributor.author | Lee, ASY | en_US |
| dc.contributor.author | Lin, CC | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:37:11Z | |
| dc.date.available | 2014-12-08T15:37:11Z | |
| dc.date.issued | 2004-12-06 | en_US |
| dc.description.abstract | The CBr4-photoirradiation in methanol generates a controlled source of HBr, which can chemoselectively deprotect commonly used hydroxyl-protecting groups in saccharides and nucleosides, such as tert-butyldimethylsilyl, isopropylidene, benzylidene and triphenyl ethers in the presence of other acid-labile functional groups. (C) 2004 Elsevier Ltd. All rights reserved. | en_US |
| dc.identifier.doi | 10.1016/j.tet.2004.09.095 | en_US |
| dc.identifier.issn | 0040-4020 | en_US |
| dc.identifier.journal | TETRAHEDRON | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/j.tet.2004.09.095 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/25557 | |
| dc.identifier.wosnumber | WOS:000225148000016 | |
| dc.language.iso | en_US | en_US |
| dc.subject | CBr4-photoirradiation | en_US |
| dc.subject | deprotection | en_US |
| dc.title | Chemoselective deprotection of acid labile primary hydroxyl protecting groups under CBr4-photoirradiation conditions | en_US |
| dc.type | Article | en_US |