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.
Aromatic nucleophilic substitution reactions of some 3-nitro-2-p-nitro-phenoxy-5-X-thiophenes with substituted anilines in methanol / Consiglio, G; Frenna, V; Guernelli, S; Macaluso, G; Spinelli, D. - In: JOURNAL OF CHEMICAL RESEARCH. SYNOPSES. - ISSN 0308-2342. - STAMPA. - 7:(2001), pp. 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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