A series of optimised 'thiophene' sigma constant values has been calculated by using the reactions of some 3-nitro-2-p-nitrophenoxy-5-X-thiophenes with some substituted anilines. The susceptibility constants obtained are discussed in the framework of the reactivity-selectivity principle.
Consiglio, G., Frenna, V., Guernelli, S., Macaluso, G., Spinelli, D. (2001). Aromatic nucleophilic substitution reactions of some 3-nitro-2-p-nitro-phenoxy-5-X-thiophenes with substituted anilines in methanol. JOURNAL OF CHEMICAL RESEARCH. SYNOPSES, 7, 266-267.
Aromatic nucleophilic substitution reactions of some 3-nitro-2-p-nitro-phenoxy-5-X-thiophenes with substituted anilines in methanol
Consiglio, G;Guernelli, S
;
2001
Abstract
A series of optimised 'thiophene' sigma constant values has been calculated by using the reactions of some 3-nitro-2-p-nitrophenoxy-5-X-thiophenes with some substituted anilines. The susceptibility constants obtained are discussed in the framework of the reactivity-selectivity principle.File in questo prodotto:
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