The CuAAC reaction was used for the development of a click approach to a series of triazole-substituted bipyridinyl derivatives. 4,4′-Diethinyl 2,2′-bipyridine and 4,4′-diazido 2,2′-bipyridine were synthesized and tested in the cycloaddition reactions. While 4,4′-diazido 2,2′-bipyridine revealed unreactive in CuAAC reactions, its corresponding N,N′-dioxide afforded the expected cycloaddition product.

A modular "Click" approach to substituted 2,2' bipyridine / P. Fabbrizzi; B. Cecconi; S. Cicchi. - In: SYNLETT. - ISSN 0936-5214. - STAMPA. - -:(2011), pp. 223-226. [10.1055/s-0030-1259304]

A modular "Click" approach to substituted 2,2' bipyridine

FABBRIZZI, PIERANGELO;CICCHI, STEFANO
2011

Abstract

The CuAAC reaction was used for the development of a click approach to a series of triazole-substituted bipyridinyl derivatives. 4,4′-Diethinyl 2,2′-bipyridine and 4,4′-diazido 2,2′-bipyridine were synthesized and tested in the cycloaddition reactions. While 4,4′-diazido 2,2′-bipyridine revealed unreactive in CuAAC reactions, its corresponding N,N′-dioxide afforded the expected cycloaddition product.
2011
-
223
226
P. Fabbrizzi; B. Cecconi; S. Cicchi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/517279
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