Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/9151
Title: Synthesis of potential fungicidal bibenzyls from bio-renewable source
Authors: Siddiqui, Ibadur R
Singh, Jaya
Singh, Pravin K
Singh, Jagdamba
Keywords: Bibenzyls
condensation
aryl amines
Schiff’s bases
neucleophilic addition
2-mercaptopropionic acid
microwave irradiation
antifungal screening
Issue Date: Jul-2005
Publisher: CSIR
Series/Report no.: Int.Cl.7 C 07 C 15/00 // A 61 P
Abstract: Acetylation of bibenzyl 1 yields 4,4'-diacetylbibenzyl 2, which on condensation with different aryl amines gives corresponding Schiff’s bases in situ. Nucleophilic addition of 2-mercaptopropionic acid or 2-mercaptosuccinic acid on Schiff’s bases followed by cyclodehydration in solvent-free condition under microwave irradiation affords 4,4'-bis(3"-aryl-2"-methyl-5"-methyl/carboxymethyl-4"-oxo-thiazolidin-2"-yl)bibenzyl 3a-n with excellent yield (88-94%). The rate of the reaction is enhanced 225 times in comparison with conventional method. Antifungal screening results on Fusarium oxysporum and Penicillium citrinum show that most of the synthesized compounds display promising antifungal activity, comparable with Griseofulvin and Dithane M-45 as standards.
Description: 1460-1464
URI: http://hdl.handle.net/123456789/9151
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.44B(07) [July 2005]

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