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Synthesis of Novel Mercaptophenyl Carbocyclic C-Nucleoside Analogue Using Sequential [3,3]-Sigmatropic Rearrangement and Ring-closing Metathesis
| Content Provider | Semantic Scholar |
|---|---|
| Author | Hee, Joon |
| Copyright Year | 2008 |
| Abstract | Novel mercaptophenyl carbocyclic C-nucleoside analogue was synthesized via a cyclopentenol intermediate 10, which was prepared using a sequential [3,3]-sigmatropic rearrangement and ring-closing metathesis (RCM). Friedel-Crafts alkylation was then used to couple the thiophenol. |
| Starting Page | 847 |
| Ending Page | 850 |
| Page Count | 4 |
| File Format | PDF HTM / HTML |
| DOI | 10.5012/bkcs.2008.29.4.847 |
| Volume Number | 29 |
| Alternate Webpage(s) | http://ocean.kisti.re.kr/downfile/volume/chemical/JCGMCS/2008/v29n4/JCGMCS_2008_v29n4_847.pdf |
| Alternate Webpage(s) | https://doi.org/10.5012/bkcs.2008.29.4.847 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |