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Each Interruption is an Opportunity: Novel Synthetic Strategies Explored Through Interrupted Click Reactions.
Brunelli, Francesca; Russo, Camilla; Giustiniano, Mariateresa; Tron, Gian Cesare.
Afiliação
  • Brunelli F; Dipartimento di Scienze del Farmaco, Università del Piemonte Orientale, Largo Donegani 2, 28100, Novara, Italy.
  • Russo C; Dipartimento di Farmacia, Università degli Studi, Federico II, Via D. Montesano 49, 80131, Napoli, Italy.
  • Giustiniano M; Dipartimento di Farmacia, Università degli Studi, Federico II, Via D. Montesano 49, 80131, Napoli, Italy.
  • Tron GC; Dipartimento di Scienze del Farmaco, Università del Piemonte Orientale, Largo Donegani 2, 28100, Novara, Italy.
Chemistry ; 30(20): e202303844, 2024 Apr 05.
Article em En | MEDLINE | ID: mdl-38408267
ABSTRACT
The particular and unique mechanism of the copper-catalyzed reaction between azides and alkynes (CuAAC) has not only allowed for the efficient synthesis of 1,2,3-trisubstituted 1,4-triazoles in excellent yields and under mild conditions, becoming the quintessential click reaction, but it has also enabled the straightforward formation of a metallocycle intermediate, the copper triazolyl. This, under suitable reaction conditions able to suppress its protonolysis, can be used either for the creation of new bicyclic triazolyl structures or for the generation of novel three or four-component reactions. The aim of this review is to rationalize and unify all these transformations, which are collectively referred to as "interrupted click reactions".
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article