2015
DOI: 10.1002/jhet.1729
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Solvent‐free One‐pot Synthesis of 2,2′‐dithioxo‐[5,5′]bithiazolidinylidene‐4,4′‐diones

Abstract: Solvent‐free one‐pot synthesis of 2,2′‐dithioxo‐[5,5′]bithiazolidinylidene‐4,4′‐dione (birhodanine) derivatives from the reaction of primary amines and carbon disulfide in the presence of dimethyl acetylene dicarboxylate has been reported.

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Cited by 20 publications
(11 citation statements)
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“…[39][40][41][42][43] The reduction of work-up procedures and purication steps, high purity of desired products, short reaction times, high to excellent yields are among the signicant benets of multicomponent one-pot reactions. 44,45 Furthermore, the reaction involving ring opening of epoxides with organic azides in water solvent occurs with perfect regioselectivity and takes advantage of green and benign conditions.…”
Section: Introductionmentioning
confidence: 99%
“…[39][40][41][42][43] The reduction of work-up procedures and purication steps, high purity of desired products, short reaction times, high to excellent yields are among the signicant benets of multicomponent one-pot reactions. 44,45 Furthermore, the reaction involving ring opening of epoxides with organic azides in water solvent occurs with perfect regioselectivity and takes advantage of green and benign conditions.…”
Section: Introductionmentioning
confidence: 99%
“…A one-step synthesis of BT-diones, reported by Nasiri, et al , reacted aliphatic primary amines with carbon disulfide and dimethylacetylene dicarboxylate ( Scheme 1 ). 21 This method produced multi-gram quantities of BT derivatives in one step without the need for chromatographic purification. There are few known functional BT derivatives 22 , 23 and no reports of BT-containing polymers.…”
Section: Introductionmentioning
confidence: 99%
“…Birhodanine derivative was synthesized according to the previously reported method with some modification . Dropwise 3–(triethoxysilyl)propan–1–amine (APTMS) (4 mmol, 0.72 g) was added to a stirred solution of carbon disulfide (4.8 mmol, 0.36 g) and dimethyl acetylene dicarboxylate (DMAD) (2 mmol, 0.28 g) in acetonitrile (4 ml) in 5 min.…”
Section: Methodsmentioning
confidence: 99%