Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 정낙신 | - |
dc.date.accessioned | 2016-08-28T11:08:32Z | - |
dc.date.available | 2016-08-28T11:08:32Z | - |
dc.date.issued | 1996 | - |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.other | OAK-12480 | - |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/228621 | - |
dc.description.abstract | Although cyclic sulfites are less reactive than their cyclic sulfate counterparts, the present work shows that cyclic sulfite 15a is a useful synthon for the convergent synthesis of carbocyclic nucleosides. Target compound 6, which represents a rigid carbocyclic nucleoside mimic of anti-HIV active 9-[2',3'-dideoxy-3'-C-(hydroxyrnethyl)-β-erythro-pentofuranosyl]adenine (3), was obtained after regioselective ring opening of 15a with adenine and radical-induced deoxygenanon of the extra hydroxyl group. Elsevier Science Ltd. | - |
dc.language | English | - |
dc.title | Use of a cyclic sulfite as an epoxide surrogate in the regioselective synthesis of a carbocyclic ring-enlarged 4′,1'a-methano oxetanocin analogue | - |
dc.type | Article | - |
dc.relation.issue | 14 | - |
dc.relation.volume | 37 | - |
dc.relation.index | SCI | - |
dc.relation.index | SCIE | - |
dc.relation.index | SCOPUS | - |
dc.relation.startpage | 2353 | - |
dc.relation.lastpage | 2356 | - |
dc.relation.journaltitle | Tetrahedron Letters | - |
dc.identifier.doi | 10.1016/0040-4039(96)00289-4 | - |
dc.identifier.scopusid | 2-s2.0-0029865955 | - |
dc.author.google | Jeong L.S. | - |
dc.author.google | Marquez V.E. | - |
dc.contributor.scopusid | 정낙신(16028528200) | - |
dc.date.modifydate | 20211210153610 | - |