2007
DOI: 10.1080/17415990701245081
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Efficient synthesis of N-substituted-N'-arylcarbonylthioureas under solvent-free conditions

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Cited by 10 publications
(4 citation statements)
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“…In our continuous approach toward developing biologically active heterocyclic synthesis via acetylenic esters-based reactions involving CH-, NH-or OH-acid compounds [30][31][32][33][34] , herein we wish to explain an expedient method for construction of some novel 2-imino-thiazolidine-4-one-5-ylidene acetate derivatives (3) from one-pot reaction between 4-phenylthiosemicarbazide (1a) and thiosemicarbazide (1b) with appropriate acetylenic esters (2) in good yields (Scheme-I).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In our continuous approach toward developing biologically active heterocyclic synthesis via acetylenic esters-based reactions involving CH-, NH-or OH-acid compounds [30][31][32][33][34] , herein we wish to explain an expedient method for construction of some novel 2-imino-thiazolidine-4-one-5-ylidene acetate derivatives (3) from one-pot reaction between 4-phenylthiosemicarbazide (1a) and thiosemicarbazide (1b) with appropriate acetylenic esters (2) in good yields (Scheme-I).…”
Section: Resultsmentioning
confidence: 99%
“…Some thiazoline-4-ones derivatives are reported as human immunodeficiency virus-1 (HIV-1) non-nucleoside reverse transcriptase inhibitors (NNRTIs) or anticancer activities and can inhibit cell division . In view of the various physiological activities of thiazolidinones, many thiazolidinone derivatives have been prepared and several new methods for the preparation of substituted thiazolidine-4-one have been recently reported [31][32][33][34] . However,these methods have several drawbacks, namely, the need for a high reaction temperature and long reaction time.…”
Section: Introductionmentioning
confidence: 99%
“…Some thiazoline derivatives show interesting anti-HIV or anticancer activities and can inhibit cell division [5][6][7][8][9][10]. Because of the various physiological activities of thiazolidinones, many thiazolidinone derivatives have been prepared and several new methods for the preparation of substituted thiazolidine-4-one have been recently reported [11,12]. Despite the synthetic importance of these methods, they commonly suffer from the need to elevated temperatures and also from long reaction times.…”
Section: Introductionmentioning
confidence: 99%
“…FBTT2 has been synthesized by Yavari et al under solvent-free conditions [44], however, the crystal structures and the electronic spectra of both FBTTs have not been reported. In order to investigate the effects of intra-and intermolecular hydrogen bonds on the photo-physical properties of FBTTs, both FBTT2 and FBTT4 were prepared and structurally and photo-physically characterized.…”
Section: Introductionmentioning
confidence: 99%