Iodine-induced cyclization reaction of endo-thioester substituted norbornenes followed by methylthio group rearrangement
| dc.citation.epage | 8212 | en_US |
| dc.citation.issue | 45 | en_US |
| dc.citation.spage | 8209 | en_US |
| dc.citation.volume | 37 | en_US |
| dc.citation.woscount | 22 | |
| dc.contributor.author | Wu, HJ | en_US |
| dc.contributor.author | Tsai, SH | en_US |
| dc.contributor.author | Chung, WS | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:02:14Z | |
| dc.date.available | 2014-12-08T15:02:14Z | |
| dc.date.issued | 1996-11-04 | en_US |
| dc.description.abstract | Treatment of the endo-thioester group substituted norbornenes 3a-3d with iodine in aqueous tetrahydrofuran at 25 degrees C gave the novel methylthio group rearranged lactonization products 4a-4d in 80% yields; iodolactonization reaction of 9 was applied to the synthesis of novel diacetal trioxa-cage compound 13. Copyright (C) 1996 Elsevier Science Ltd | en_US |
| dc.identifier.doi | 10.1016/0040-4039(96)01869-2 | en_US |
| dc.identifier.issn | 0040-4039 | en_US |
| dc.identifier.journal | TETRAHEDRON LETTERS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/0040-4039(96)01869-2 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/933 | |
| dc.identifier.wosnumber | WOS:A1996VR55300041 | |
| dc.language.iso | en_US | en_US |
| dc.title | Iodine-induced cyclization reaction of endo-thioester substituted norbornenes followed by methylthio group rearrangement | en_US |
| dc.type | Article | en_US |