Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 정낙신 | * |
dc.contributor.author | 김대기 | * |
dc.date.accessioned | 2017-01-05T02:01:08Z | - |
dc.date.available | 2017-01-05T02:01:08Z | - |
dc.date.issued | 2004 | * |
dc.identifier.issn | 0968-0896 | * |
dc.identifier.other | OAK-1845 | * |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/233639 | - |
dc.description.abstract | The present work describes the asymmetric synthesis of D- and L-apio-2′,3′-dideoxynucleoside analogues, 4 and 5 with 2′-hydroxyl group via a common intermediate 9, starting from D-galactose. Stereoselective dihydroxylation and deoxygenation through radical inversion were successfully employed to synthesize the key intermediate 12 with D-apio structure, while stereoselecetive hydroboration-oxidation was used for the synthesis of another key intermediate 18 with L-apio structure. © 2003 Elsevier Ltd. All rights reserved. | * |
dc.language | English | * |
dc.title | Synthesis of D- and L-apio nucleoside analogues with 2′-hydroxyl group as potential anti-HIV agents | * |
dc.type | Article | * |
dc.relation.issue | 5 | * |
dc.relation.volume | 12 | * |
dc.relation.index | SCI | * |
dc.relation.index | SCIE | * |
dc.relation.index | SCOPUS | * |
dc.relation.startpage | 1101 | * |
dc.relation.lastpage | 1109 | * |
dc.relation.journaltitle | Bioorganic and Medicinal Chemistry | * |
dc.identifier.doi | 10.1016/j.bmc.2003.12.002 | * |
dc.identifier.wosid | WOS:000189314700028 | * |
dc.identifier.scopusid | 2-s2.0-1342321885 | * |
dc.author.google | Jin D.Z. | * |
dc.author.google | Kwon S.H. | * |
dc.author.google | Moon H.R. | * |
dc.author.google | Gunaga P. | * |
dc.author.google | Kim H.O. | * |
dc.author.google | Kim D.-K. | * |
dc.author.google | Chun M.W. | * |
dc.author.google | Jeong L.S. | * |
dc.contributor.scopusid | 정낙신(16028528200) | * |
dc.contributor.scopusid | 김대기(35083694200) | * |
dc.date.modifydate | 20240118164500 | * |