2003
DOI: 10.1002/jhet.5570400427
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Synthesis of some furo‐thiazolidine derivatives starting from aldimines

Abstract: Alkyl and aryl substituted furothiazolidine derivatives have been synthesized by the reaction of Wittig reagent with benzylidene derivatives of 4‐thiazolidinones obtained from aldimines and thioglicolic acid.

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Cited by 30 publications
(11 citation statements)
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“…The mixture was refluxed (18)(19)(20) h. After completion of the reaction, the product was cooled to room temperature and the benzene was removed under vacuum [21]. The whole mass treated with saturated solution of sodium bicarbonate until carbon dioxide evolution.…”
Section: Synthesis Of 2-[6-(4-chlorobenzyloxy)naphthyl-3-(4-substitutmentioning
confidence: 99%
See 1 more Smart Citation
“…The mixture was refluxed (18)(19)(20) h. After completion of the reaction, the product was cooled to room temperature and the benzene was removed under vacuum [21]. The whole mass treated with saturated solution of sodium bicarbonate until carbon dioxide evolution.…”
Section: Synthesis Of 2-[6-(4-chlorobenzyloxy)naphthyl-3-(4-substitutmentioning
confidence: 99%
“…The traditional methods reported can be either a one-pot three-component condensation [15] or in two-step transform. In the current study, 4-thiazolidinones have been synthesized in two steps, the first step included condensation of substituted-2-naphthaldehyde with various substituted aromatic amines and formation of an imine, which undergoes attack by generated sulfur nucleo-phile, followed by intramolecular cyclization on disposal of water in the second step [16][17][18].…”
Section: Introductionmentioning
confidence: 99%
“…The main synthetic routes for 1,3-thiazolidin-4-ones involve a threecomponent reaction between an amine, a carbonyl compound, and thioglycolic acid. [44][45][46] The newest methodology is synthesis of bis-thiazolidinones through multicomponent reaction of aldehydes, ethylenediamine, and thioglycolic acid using (a) nano-CdZr 4 (PO 4 ) 6 [47] and (b) chitosan-attached nano-CuFe 2 O 4 , [48] and synthesis of oxindole derivatives containing thiazolidinone using nano silica-bonded 5-n-propyl-octahydro-pyrimido [1,2-a] azepiniumchloride via a one-pot reaction of 5-oxoindolinylidene rhodanine-3-acetic acid derivatives, 2-aminothiophenol, and triphenyl phosphite. [49] Mesoporous silicas are inorganic materials formed by the condensation of sodium silicate or silicon alkoxides around an ordered surfactant used as template.…”
Section: Introductionmentioning
confidence: 99%
“…Their synthesis can be either a one‐pot three‐component condensation or a two‐step process. The reactions involved formation of an imine first, which attacked by sulfur nucleophile, and then, intramolecular cyclization and elimination of water occurred .…”
Section: Introductionmentioning
confidence: 99%