1,4-Benzodithians, when treated with bromine in anhydrous chloroform, undergo very fast monobromination at the aromatic ring. By the use of quantum mechanical semiempirical calculations, the reaction is shown to proceed most likely via a vicarious nucleophilic substitution of hydrogen

Chemistry of ethanediyl S,S-Acetals 6 – An example of vicarious nucleophilic substitution of hydrogen in 1,4-benzodithians / R., Caputo; M., De Nisco; Palumbo, Giovanni; C., Adamo; V., Barone. - In: TETRAHEDRON. - ISSN 0040-4020. - STAMPA. - 49:48(1993), pp. 11383-11388. [10.1016/S0040-4020(01)81819-6]

Chemistry of ethanediyl S,S-Acetals 6 – An example of vicarious nucleophilic substitution of hydrogen in 1,4-benzodithians

PALUMBO, GIOVANNI;
1993

Abstract

1,4-Benzodithians, when treated with bromine in anhydrous chloroform, undergo very fast monobromination at the aromatic ring. By the use of quantum mechanical semiempirical calculations, the reaction is shown to proceed most likely via a vicarious nucleophilic substitution of hydrogen
1993
Chemistry of ethanediyl S,S-Acetals 6 – An example of vicarious nucleophilic substitution of hydrogen in 1,4-benzodithians / R., Caputo; M., De Nisco; Palumbo, Giovanni; C., Adamo; V., Barone. - In: TETRAHEDRON. - ISSN 0040-4020. - STAMPA. - 49:48(1993), pp. 11383-11388. [10.1016/S0040-4020(01)81819-6]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/475713
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