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Cited by 3 publications
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“…Triflamide was successfully subjected to the amidoalkylation reaction with N -(2,2,2-trichloroethylidene)triflamide CF 3 SO 2 NH 2 + CF 3 SO 2 normalNC HCCl 3 false( CF 3 SO 2 NH false) 2 CHCCl 3 It is worth mentioning that nonfluorinated analogues of triflamide, like ArSO 2 NCHCCl 3 , do not enter this reaction …”
Section: Trifluoromethanesulfonamides (Triflamides)mentioning
confidence: 99%
“…Triflamide was successfully subjected to the amidoalkylation reaction with N -(2,2,2-trichloroethylidene)triflamide CF 3 SO 2 NH 2 + CF 3 SO 2 normalNC HCCl 3 false( CF 3 SO 2 NH false) 2 CHCCl 3 It is worth mentioning that nonfluorinated analogues of triflamide, like ArSO 2 NCHCCl 3 , do not enter this reaction …”
Section: Trifluoromethanesulfonamides (Triflamides)mentioning
confidence: 99%
“…Polyfunctionsl halogen-containing ethylamides of sulfonic acids are initial compounds for preparation of amino acids [8], amidine derivatives of amino acids [9], and heterocyclic compounds [10,11]. Polyfunctionsl halogen-containing ethylamides of sulfonic acids are initial compounds for preparation of amino acids [8], amidine derivatives of amino acids [9], and heterocyclic compounds [10,11].…”
mentioning
confidence: 99%