Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chou, Chu-En | en_US |
dc.contributor.author | Chen, Yi-An | en_US |
dc.contributor.author | Lin, Yi-Ching | en_US |
dc.contributor.author | Kao, Shih-Chieh | en_US |
dc.contributor.author | Chang, Chieh-Yu | en_US |
dc.contributor.author | Wu, Yen-Ku | en_US |
dc.date.accessioned | 2020-10-05T02:02:00Z | - |
dc.date.available | 2020-10-05T02:02:00Z | - |
dc.date.issued | 1970-01-01 | en_US |
dc.identifier.issn | 0009-4536 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1002/jccs.202000216 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/155413 | - |
dc.description.abstract | Described is a formal synthesis of racemic schulzeines B and C that intercepts intermediates developed by Gurjar and co-workers. The synthetic sequence features an annulative coupling of a ketimine and acrylic acid enabling the construction of the benzoquinolizidine nucleus in a highly convergent manner. We also examined a continuous-flow version of the thermal aza-annulation, which proved less practical as compared to the batch processes. | en_US |
dc.language.iso | en_US | en_US |
dc.subject | 2-piperidone | en_US |
dc.subject | aza-annulation | en_US |
dc.subject | benzoqionolizidine | en_US |
dc.subject | marine alkaloid | en_US |
dc.subject | schulzeine | en_US |
dc.title | Formal synthesis of schulzeines B and C: A new route to Gurjar's lactams | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1002/jccs.202000216 | en_US |
dc.identifier.journal | JOURNAL OF THE CHINESE CHEMICAL SOCIETY | en_US |
dc.citation.spage | 0 | en_US |
dc.citation.epage | 0 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000561018200001 | en_US |
dc.citation.woscount | 0 | en_US |
Appears in Collections: | Articles |