Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 윤주영 | * |
dc.date.accessioned | 2017-01-05T02:01:17Z | - |
dc.date.available | 2017-01-05T02:01:17Z | - |
dc.date.issued | 2003 | * |
dc.identifier.issn | 0040-4020 | * |
dc.identifier.other | OAK-1614 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/233703 | - |
dc.description.abstract | Paclitaxel analogues with a thiol group in place of the hydroxyl group on the C-13 side-chain constitute an interesting avenue of research for the study of new taxoid compounds. A synthetic route for the preparation of 2′-deoxy-2′-epi-mercaptopaclitaxel with high ee has been developed. The key step is the regio-controlled ring-opening reaction of the trans-oxazoline derivative with thiolacetic acid, which allows the introduction of the sulfur-containing group onto the side-chain. © 2003 Elsevier Ltd. All rights reserved. | * |
dc.language | English | * |
dc.title | Synthesis of novel taxoid analogue containing sulfur group on C-13 side-chain: 2′-deoxy-2′-epi-mercaptopaclitaxel | * |
dc.type | Article | * |
dc.relation.issue | 37 | * |
dc.relation.volume | 59 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 7409 | * |
dc.relation.lastpage | 7412 | * |
dc.relation.journaltitle | Tetrahedron | * |
dc.identifier.doi | 10.1016/S0040-4020(03)01098-6 | * |
dc.identifier.wosid | WOS:000185310700019 | * |
dc.identifier.scopusid | 2-s2.0-0042382887 | * |
dc.author.google | Qi X. | * |
dc.author.google | Lee S.-H. | * |
dc.author.google | Yoon J. | * |
dc.author.google | Lee Y.-S. | * |
dc.contributor.scopusid | 윤주영(7403587371) | * |
dc.date.modifydate | 20240118162450 | * |