Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 이상국 | - |
dc.date.accessioned | 2018-05-02T08:15:43Z | - |
dc.date.available | 2018-05-02T08:15:43Z | - |
dc.date.issued | 2004 | - |
dc.identifier.issn | 0022-3263 | - |
dc.identifier.other | OAK-2153 | - |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/242780 | - |
dc.description.abstract | The asymmetric total syntheses of the representative phenanthroindolizidine and phenanthroquinolizidine alkaloids, (-)-antofine and (-)-cryptopleurine, are described. An efficient synthetic pathway to the key intermediate 12, in enantiomerically pure form, was achieved by using a chiral building block (R)-9 and the Overman rearrangement with a total transfer of chirality. The problem of constructing the pyrrolidine and piperidine rings was successfully addressed, primarily by using a ring-closing metathesis reaction and a cross-metathesis reaction, respectively. | - |
dc.language | English | - |
dc.title | Asymmetric Total Syntheses of (-)-Antofine and (-)-Cryptopleurine Using (R)-(E)-4-(Tributylstannyl)but-3-en-2-ol | - |
dc.type | Article | - |
dc.relation.issue | 9 | - |
dc.relation.volume | 69 | - |
dc.relation.index | SCI | - |
dc.relation.index | SCIE | - |
dc.relation.index | SCOPUS | - |
dc.relation.startpage | 3144 | - |
dc.relation.lastpage | 3149 | - |
dc.relation.journaltitle | Journal of Organic Chemistry | - |
dc.identifier.doi | 10.1021/jo049820a | - |
dc.identifier.wosid | WOS:000221268200029 | - |
dc.identifier.scopusid | 2-s2.0-2142711603 | - |
dc.author.google | Kim S. | - |
dc.author.google | Lee T. | - |
dc.author.google | Lee E. | - |
dc.author.google | Lee J. | - |
dc.author.google | Fan G.-J. | - |
dc.author.google | Lee S.K. | - |
dc.author.google | Kim D. | - |
dc.contributor.scopusid | 이상국(36067620500) | - |
dc.date.modifydate | 20211210153309 | - |