Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3668
Title: Electrophilic substitution reactions of trisheteroarylmethanes: an efficient strategy to develop novel synthons for organic synthesis
Authors: Vijay Nair, G
Siji Thomas
Smitha C Mathew
Vidya, N
Rath, N P
Keywords: Tris-thienylmethane
Tris-furylmethane
Furanone
Butenolides
Issue Date: 2005
Publisher: Pergamon-Elsevier Science
Citation: Tetrahedron 61(40):9533-9540; 3 Oct 2005
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.
URI: http://hdl.handle.net/123456789/3668
ISSN: 0040-4020
Appears in Collections:2005

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