Nair, Vijay ; Thomas, Siji ; Mathew, Smitha C. ; Vidya, N. ; Rath, Nigam P. (2005) Electrophilic substitution reactions of trisheteroarylmethanes: an efficient strategy to develop novel synthons for organic synthesis Tetrahedron, 61 (40). pp. 9533-9540. ISSN 0040-4020
Full text not available from this repository.
Official URL: http://www.sciencedirect.com/science/article/pii/S...
Related URL: http://dx.doi.org/10.1016/j.tet.2005.07.092
Abstract
Trisheteroarylmethanes are interesting molecules for the construction of three dimensionally complex systems. From this vantage point, we studied electrophilic substitution reactions on tris-2-thienylmethane and tris-2-furylmethane. During the bromination reaction, we have isolated the tris-bromosubstituted tris-2-thienylmethane in the former case and brominated furanones in the latter case, which may be of synthetic and biological importance.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to Elsevier Science. |
| Keywords: | Tris-thienylmethane; Tris-furylmethane; Furanone; Butenolides |
| ID Code: | 84098 |
| Deposited On: | 24 Feb 2012 06:15 |
| Last Modified: | 24 Feb 2012 06:15 |
Repository Staff Only: item control page
