Joined use of oxazolidinone and desymmetric amino protection: a new strategy for protection of glucosamine
| dc.citation.epage | 1913 | en_US |
| dc.citation.issue | 14 | en_US |
| dc.citation.spage | 1910 | en_US |
| dc.citation.volume | 51 | en_US |
| dc.citation.woscount | 4 | |
| dc.contributor.author | Lin, Shih-Che | en_US |
| dc.contributor.author | Chao, Chin-Sheng | en_US |
| dc.contributor.author | Chang, Chiu-Ching | en_US |
| dc.contributor.author | Mong, Kwok-Kong T. | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:07:03Z | |
| dc.date.available | 2014-12-08T15:07:03Z | |
| dc.date.issued | 2010-04-07 | en_US |
| dc.description.abstract | Joined use of N-benzyl oxazolidinone and N-benzyl-N-benzyloxycarbonyl (N-BnCbz) desymmetric amino-protecting function is reported. The new synthetic approach enables the facile preparation of type I and type 2 LacNAc disaccharides in satisfactory yields. One-pot deprotection of N-BnCbz and O-benzyl ether is achieved by hydrogenolysis under mild conditions. (C) 2010 Elsevier Ltd. All rights reserved. | en_US |
| dc.identifier.doi | 10.1016/j.tetlet.2010.02.021 | en_US |
| dc.identifier.issn | 0040-4039 | en_US |
| dc.identifier.journal | TETRAHEDRON LETTERS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/j.tetlet.2010.02.021 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/5522 | |
| dc.identifier.wosnumber | WOS:000275920600026 | |
| dc.language.iso | en_US | en_US |
| dc.title | Joined use of oxazolidinone and desymmetric amino protection: a new strategy for protection of glucosamine | en_US |
| dc.type | Article | en_US |