| Title: | Iodine-induced cyclization reaction of endo-thioester substituted norbornenes followed by methylthio group rearrangement |
| Authors: | Wu, HJ Tsai, SH Chung, WS 應用化學系 Department of Applied Chemistry |
| Issue Date: | 4-Nov-1996 |
| 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 |
| URI: | http://dx.doi.org/10.1016/0040-4039(96)01869-2 http://hdl.handle.net/11536/933 |
| ISSN: | 0040-4039 |
| DOI: | 10.1016/0040-4039(96)01869-2 |
| Journal: | TETRAHEDRON LETTERS |
| Volume: | 37 |
| Issue: | 45 |
| Begin Page: | 8209 |
| End Page: | 8212 |
| Appears in Collections: | Articles |
Files in This Item:
If it is a zip file, please download the file and unzip it, then open index.html in a browser to view the full text content.
- A novel iodine-induced sequential cyclization reaction of norbornene derivatives leading to the formation of novel iodo-cage compounds / Wu, HJ;Tsai, SH;Chung, WS
- Synthesis of diacetal trioxa-cage compounds via a sequential cyclization reaction of norbornene derivatives induced by electrophiles / Wu, HJ;Tsai, SH;Chern, JH;Lin, HC
- Stereoselectivity of the Diels-Alder reaction of (E)gamma-Oxo-alpha,beta-unsaturated thioesters with cyclopentadiene / Tsai, SH;Chung, WS;Wu, HJ
Loading...