1997
DOI: 10.1039/a703033i
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Reaction of trithiazyl trichloride with active methylene compounds

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Cited by 17 publications
(16 citation statements)
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“…The physical and spectroscopic properties of 1a, [10] 2a, [11] and 2b [12] are in good agreement with previous reports. These properties are listed in the Supplementary Material.…”
Section: Synthesissupporting
confidence: 90%
“…The physical and spectroscopic properties of 1a, [10] 2a, [11] and 2b [12] are in good agreement with previous reports. These properties are listed in the Supplementary Material.…”
Section: Synthesissupporting
confidence: 90%
“…179 Activated methylene compounds similarly give disubstituted 1,2,5-thiadiazoles; thus, the thiadiazole 118 was isolated (41%) from a reaction with dibenzoylmethane. 180 More exotic structures are obtained from reactions of trithiazyl View Online chloride with pyrroles; an example is the bis(thiadiazole) 119 formed (45%) with 1-methyl-2,5-diphenylpyrrole. 181 1,2,5-Thiadiazoles have also been isolated in moderate yield from the reaction of tetrasulfur tetranitride or its antimony() chloride complex with oximes 182,183 and with isoxazoles.…”
Section: Oxadiazoles and Thiadiazolesmentioning
confidence: 99%
“…With trisubstituted ethene (Z)-ethyl 4-phenyl-3-benzylbut-2-enoate debenzylation takes place giving 4-phenyl-1,2,5-thiadiazole-3-carboxylate. 83 Also this method provided a new and efficient two-step route to 3-amino-1,2,5-thiadiazole starting from Nvinylphthalimide, 85 overcoming a problematic multi-step synthesis from aminoacetamidine and sulfur monochloride. 35…”
Section: Scheme 38mentioning
confidence: 99%
“…Treatment of ethenes with [(NSCl) 3 ] in benzene at reflux afforded 1,2,5-thiadiazoles 83 in moderate to good yields (Scheme 39). 83,85,86 The reaction may undergo the chlorination at allylic or benzylic positions, especially if excess of the trimer is used. With trisubstituted ethene (Z)-ethyl 4-phenyl-3-benzylbut-2-enoate debenzylation takes place giving 4-phenyl-1,2,5-thiadiazole-3-carboxylate.…”
Section: Scheme 38mentioning
confidence: 99%