Synthesis of cryptolepine and cryptoteckieine from a common intermediate
| dc.citation.epage | 3827 | en_US |
| dc.citation.issue | 11 | en_US |
| dc.citation.spage | 3823 | en_US |
| dc.citation.volume | 85 | en_US |
| dc.citation.woscount | 35 | |
| dc.contributor.author | Ho, TL | en_US |
| dc.contributor.author | Jou, DG | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:42:54Z | |
| dc.date.available | 2014-12-08T15:42:54Z | |
| dc.date.issued | 2002 | en_US |
| dc.description.abstract | Both cryptolepine 1 and cryptotackieine 3 have been synthesized from 1,3-bis(2-nitrophenyl)propan-2-one. The approach to 1 involved reduction of the NO2 groups, oxidative cyclization with Phl(OAc)(2), and N-methylation, whereas 3 was obtained via bromination, Favorskii rearrangement, reduction (in situ cyclization), and N-methylation. | en_US |
| dc.identifier.doi | 10.1002/1522-2675(200211)85:11<3823 | en_US |
| dc.identifier.issn | 0018-019X | en_US |
| dc.identifier.journal | HELVETICA CHIMICA ACTA | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1002/1522-2675(200211)85:11<3823 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/29077 | |
| dc.identifier.wosnumber | WOS:000179932000016 | |
| dc.language.iso | en_US | en_US |
| dc.title | Synthesis of cryptolepine and cryptoteckieine from a common intermediate | en_US |
| dc.type | Article | en_US |