LiNTf2 in the reaction of lactones with amines is able to activate cyclic esters towards ring opening, thus leading to clean open-chain amides under mild conditions and using a stoichiometric amount of amine. The generality of the method was demonstrated by a range of selected lactones and amines.

LiNTf2-Catalyzed aminolysis of lactones with stoichiometric quantities of amines / Lalli, C.; Trabocchi, Andrea; Menchi, Gloria; Guarna, Antonio. - In: SYNLETT. - ISSN 0936-5214. - STAMPA. - --:(2008), pp. 189-192. [10.1055/s-2007-1000882]

LiNTf2-Catalyzed aminolysis of lactones with stoichiometric quantities of amines

TRABOCCHI, ANDREA;MENCHI, GLORIA;GUARNA, ANTONIO
2008

Abstract

LiNTf2 in the reaction of lactones with amines is able to activate cyclic esters towards ring opening, thus leading to clean open-chain amides under mild conditions and using a stoichiometric amount of amine. The generality of the method was demonstrated by a range of selected lactones and amines.
2008
--
189
192
Lalli, C.; Trabocchi, Andrea; Menchi, Gloria; Guarna, Antonio
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/253006
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