Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 정낙신 | - |
dc.date.accessioned | 2018-05-02T08:15:56Z | - |
dc.date.available | 2018-05-02T08:15:56Z | - |
dc.date.issued | 2004 | - |
dc.identifier.issn | 0022-3263 | - |
dc.identifier.other | OAK-2100 | - |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/242838 | - |
dc.description.abstract | The preparative and stereoselective synthesis (45-50% overall yields) of the target compound 17 has been accomplished from D-ribose. The bulky protecting groups such as TBDPS and Trityl enforced the facial selectivity during Grignard reaction to give the tertiary β-allylic alcohol 16 as the sole product, which was oxidatively rearranged to the key molecule 17 in excellent yield. | - |
dc.language | English | - |
dc.title | Preparative and Stereoselective Synthesis of the Versatile Intermediate for Carbocyclic Nucleosides: Effects of the Bulky Protecting Groups to Enforce Facial Selectivity | - |
dc.type | Article | - |
dc.relation.issue | 7 | - |
dc.relation.volume | 69 | - |
dc.relation.index | SCI | - |
dc.relation.index | SCIE | - |
dc.relation.index | SCOPUS | - |
dc.relation.startpage | 2634 | - |
dc.relation.lastpage | 2636 | - |
dc.relation.journaltitle | Journal of Organic Chemistry | - |
dc.identifier.doi | 10.1021/jo0356762 | - |
dc.identifier.wosid | WOS:000220506200066 | - |
dc.identifier.scopusid | 2-s2.0-1842607464 | - |
dc.author.google | Choi W.J. | - |
dc.author.google | Moon H.R. | - |
dc.author.google | Kim H.O. | - |
dc.author.google | Yoo B.N. | - |
dc.author.google | Lee J.A. | - |
dc.author.google | Shin D.H. | - |
dc.author.google | Jeong L.S. | - |
dc.contributor.scopusid | 정낙신(16028528200) | - |
dc.date.modifydate | 20211210153610 | - |