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Recent Progress in Catalytic Synthesis of 1,2,3-Triazoles
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Algieri, Vincenzo
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Univ Calabria, Dipartimento Chim & Tecnol Chim, Via P Bucci,Cubo 12-C, I-87036 Arcavacata Di Rende, CS, Italy Univ Calabria, Dipartimento Chim & Tecnol Chim, Via P Bucci,Cubo 12-C, I-87036 Arcavacata Di Rende, CS, Italy

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Tallarida, Matteo Antonio
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Univ Calabria, Dipartimento Chim & Tecnol Chim, Via P Bucci,Cubo 12-C, I-87036 Arcavacata Di Rende, CS, Italy Univ Calabria, Dipartimento Chim & Tecnol Chim, Via P Bucci,Cubo 12-C, I-87036 Arcavacata Di Rende, CS, Italy
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[1] Univ Calabria, Dipartimento Chim & Tecnol Chim, Via P Bucci,Cubo 12-C, I-87036 Arcavacata Di Rende, CS, Italy
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关键词:
1;
2;
3-triazoles;
click chemistry;
3-dipolar cycloaddition;
Huisgen reactions;
triazole synthesis;
AZIDE-ALKYNE CYCLOADDITION;
METAL-FREE ROUTE;
REGIOSELECTIVE SYNTHESIS;
ONE-POT;
1,5-DISUBSTITUTED 1,2,3-TRIAZOLES;
1,3-DIPOLAR CYCLOADDITION;
IONIC LIQUID;
1,4-DISUBSTITUTED 1,2,3-TRIAZOLES;
MULTICOMPONENT REACTION;
BIOLOGICAL EVALUATION;
D O I:
10.3390/catal11091120
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
1,2,3-triazoles represent a functional heterocyclic core that has been at the center of modern organic chemistry since the beginning of click chemistry. Being a versatile framework, such an aromatic ring can be observed in uncountable molecules useful in medicine and photochemistry, just to name a few. This review summarizes the progress achieved in their synthesis from 2015 to today, with particular emphasis on the development of new catalytic and eco-compatible approaches. In doing so, we subdivided the report based on their degree of functionalization and, for each subparagraph, we outlined the role of the catalyst employed.
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Univ Tours, UMR GICC Equipe Innovat Mol & Therapeut 7292 4, Labex SYNORG, Fac Pharm, 31 Ave Monge, F-37200 Tours, France Univ Tours, UMR GICC Equipe Innovat Mol & Therapeut 7292 4, Labex SYNORG, Fac Pharm, 31 Ave Monge, F-37200 Tours, France