Solvolyses of thiocyanates by trifluoroethanoic acid
RD Gillard, N Garif, JP de Jesus
Index: Gillard, R. D.; Garif, Nordin; Pedrosa De Jesus, Julio Polyhedron, 1989 , vol. 8, p. 775 - 792
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Abstract
Abstract The solvolyses by trifluoroethanoic (“trifluoroacetic” TFA) acid of several known and new thiocyanates have been studied using proton magnetic resonance. For the organic linkage isomers of RNCS (R= alkyl groups) isothiocyanates react (via N-alkyl monothiocarbamato trifluoroethanoates) to form alkylamines RNH 2, whereas the thiocyanates RSCN yield thiols, RSH and ammonia. The coordinated thiocyanates include ...
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