Iterative click reactions using trivalent platforms for sequential molecular assembly.
Chem Commun (Camb)
; 60(45): 5824-5827, 2024 May 30.
Article
em En
| MEDLINE
| ID: mdl-38747212
ABSTRACT
A facile synthesis of multi(triazole)s by iterative click reactions is disclosed. Good functional group tolerance of sequential click assembly by sulfur-fluoride exchange (SuFEx), copper-catalyzed azide-alkyne cycloaddition (CuAAC), and thia-Michael reaction realizes the iterative click reactions. Diverse multi(triazole)-type mid-molecules can be synthesized easily from readily available modules through good chemoselective reactions without functional group transformation steps.
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Chem Commun (Camb)
/
Chem. commun. (Lond., 1996, Online)
/
Chemical communications (London. 1996. Online)
Ano de publicação:
2024
Tipo de documento:
Article