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Synthesis of 4-substituted oxazolo[4,5-c]quinolines by direct reaction at the C-4 position of oxazoles.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Akula, Mahesh Thigulla, Yadagiri Davis, Connor Race Jha, Mukund Bhattacharya, Anupam |
| Copyright Year | 2015 |
| Abstract | A facile synthesis of 4-aryl substituted oxazolo[4,5-c]quinolines has been described via a modified Pictet-Spengler method and using Cu(TFA)2 as a catalyst. The developed methodology directly functionalizes the C-4 position of oxazoles without the aid of any prefunctionalization, in the presence of the more reactive C-2 position in good yields. The versatility of the established method has been demonstrated by its application in the synthesis of 4-substituted oxazolo-[1,8]naphthyridine ring systems. |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/c4ob02224f |
| PubMed reference number | 25574832 |
| Journal | Medline |
| Volume Number | 13 |
| Issue Number | 9 |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/ob/c4/c4ob02224f/c4ob02224f1.pdf |
| Alternate Webpage(s) | https://doi.org/10.1039/c4ob02224f |
| Journal | Organic & biomolecular chemistry |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |