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

dc.contributor.author	Vijay Nair, G
dc.contributor.author	Siji Thomas
dc.contributor.author	Smitha C Mathew
dc.contributor.author	Vidya, N
dc.contributor.author	Rath, N P
dc.date.accessioned	2021-02-08T13:39:09Z
dc.date.available	2021-02-08T13:39:09Z
dc.date.issued	2005
dc.identifier.citation	Tetrahedron 61(40):9533-9540; 3 Oct 2005	en_US
dc.identifier.issn	0040-4020
dc.identifier.uri	http://hdl.handle.net/123456789/3668
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.publisher	Pergamon-Elsevier Science	en_US
dc.subject	Tris-thienylmethane	en_US
dc.subject	Tris-furylmethane	en_US
dc.subject	Furanone	en_US
dc.subject	Butenolides	en_US
dc.title	Electrophilic substitution reactions of trisheteroarylmethanes: an efficient strategy to develop novel synthons for organic synthesis	en_US
dc.type	Article	en_US