Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 정낙신 | - |
dc.date.accessioned | 2016-08-28T12:08:16Z | - |
dc.date.available | 2016-08-28T12:08:16Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.other | OAK-8696 | - |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/222575 | - |
dc.description.abstract | Fluoro-homoneplanocin A (4) was synthesized from d-ribose, via the enyne ring-closing metathesis of 9, the stereoselective opening of epoxide 23a with fluoride, and a simultaneous oxidation-elimination reaction. The key intermediate 8 is expected to serve as a versatile intermediate for the synthesis of carbanucleosides. © 2012 American Chemical Society. | - |
dc.language | English | - |
dc.title | Stereoselective synthesis of fluoro-homoneplanocin A as a potential antiviral agent | - |
dc.type | Article | - |
dc.relation.issue | 8 | - |
dc.relation.volume | 14 | - |
dc.relation.index | SCI | - |
dc.relation.index | SCIE | - |
dc.relation.index | SCOPUS | - |
dc.relation.startpage | 2134 | - |
dc.relation.lastpage | 2137 | - |
dc.relation.journaltitle | Organic Letters | - |
dc.identifier.doi | 10.1021/ol300667q | - |
dc.identifier.wosid | WOS:000302990100047 | - |
dc.identifier.scopusid | 2-s2.0-84860195223 | - |
dc.author.google | Chandra G. | - |
dc.author.google | Majik M.S. | - |
dc.author.google | Lee J.Y. | - |
dc.author.google | Jeong L.S. | - |
dc.contributor.scopusid | 정낙신(16028528200) | - |
dc.date.modifydate | 20211210153610 | - |