Phenyl-substituted N,N-dimethylanilines, synthesized by Suzuki coupling reactions in good yields, are transformed to their corresponding arylic carbanions by reductive C-N cleavage with lithium at room temperature. These carbanions react with various electrophiles affording the corresponding ipso-substituted products with absolute regioselectivity
Reactivity of Arylic Carbanions Generated by Reductive Cleavage of C-N Bond of N,N-Dimethylanilines / Azzena, Ugo Gavino; Cattari, M.; Melloni, G.; Pisano, Luisa. - In: SYNTHESIS. - ISSN 0039-7881. - 18(2003), pp. 2811-2814. [10.1055/s-2003-42481]
Reactivity of Arylic Carbanions Generated by Reductive Cleavage of C-N Bond of N,N-Dimethylanilines
AZZENA, Ugo Gavino;PISANO, Luisa
2003-01-01
Abstract
Phenyl-substituted N,N-dimethylanilines, synthesized by Suzuki coupling reactions in good yields, are transformed to their corresponding arylic carbanions by reductive C-N cleavage with lithium at room temperature. These carbanions react with various electrophiles affording the corresponding ipso-substituted products with absolute regioselectivityFile in questo prodotto:
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