Electrophilic substitution reactions of trisheteroarylmethanes: an efficient strategy to develop novel synthons for organic synthesis

Autor:	Siji Thomas, N. Vidya, Nigam P. Rath, Vijay Nair, Smitha C. Mathew
Rok vydání:	2005
Předmět:	Substitution reaction Electrophilic substitution chemistry.chemical_compound chemistry Vantage point Organic Chemistry Drug Discovery Synthon Organic chemistry Halogenation Molecule Organic synthesis Biochemistry
Zdroj:	Tetrahedron. 61:9533-9540
ISSN:	0040-4020
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::b8dbb3e623b64af74f1c898345e4dc7c https://doi.org/10.1016/j.tet.2005.07.092 Zobrazit plný text záznamu Full Text from ScienceDirect