Figure 1
Structure of isomeric Triazoles.
Figure 2
Different regioisomers of carbon and nitrogen substituted 1,2,3-triazoles.
Figure 3
Different tautomers of substituted and unsubistitued 1,2,3-triazoles.
Figure 4
Major approaches toward the - Synthesis of the 1,2,3-triazole skeleton already functionalized in N2
Figure 5
Schematic representation of monocyclic rearrangement of heterocycles.
Figure 6
Examples of molecules obtained through the Boulton-Katritzky rearrangement of oxadiazoles.
Figure 7
Synthesis of symmetric N2 substituted 1,2,3-triazoles from Aryl-Hydrazones.
Figure 8
Intramolecular copper catalyzed cyclization of β-ketohydrazones for the synthesis of N2-Aryl-1,2,3-Triazoles
Figure 9
The synthesis of 2-aryl-5-amino-1,2,3-triazoles from α-hydrazono-nitriles.
Figure 10
The copper catalyzed oxidative cyclization between oximes and diazo compounds for the synthesis of N2-PMB-1,2,3-triazoles.
Figure 11
Synthesis of hydroxymethyl-1,2,3-triazoles.
Figure 12
I- Regioselective alkylation reaction with a 4.5-dibromo-1,2,3-triazole; II-Examples of the transformtion of the N2-Alkyl-4,5-dibromo-1,2,3-triazole into N2-Alkyl-4,5-alkyl(Aryl)-1,2,3-triazoles.
Figure 13
Arylation of 4,5-dibromo-1,2,3-triazole with electron deficient arenes and heteroarenes.
Figure 14
Complete N2-Regioselective arylation of 4,5-dissubstitued 1,2,3-triazoles with chloro-nitro Benzene.
Figure 15
Highly N2regioselective Alkylation of 5-(4-Metoxi)-Phenyl-4-fluoro-1,2,3-triazole.
Figure 16
The regio and enantioselectiveaza-Michael reaction of 4-aryl-NH-1,2,3-triazoles to cyclic enones.
Figure 17
Regioselective cross-dehydrogenative coupling (CDC) between NH-1,2,3-triazoles and N,N-dialkylamides.
Figure 18
N2-regioselective autocatalytic ditriazolylation reaction of cyclopropenones with N1-sulfonyl-1,2,3-triazoles.
Figure 19
Proposed autocatalytic mechanism for the ditriazolylation reaction of cyclopropenones.
Figure 20
The Palladium Catalyzed N2-regioselective Arylation of 1,2,3-triazoles.
Figure 21
a) The 2’ Halogenation of 2-aryl-1,2,3-triazoles. b) A simplified catalytic cycle showing the ortho-palladation directing ability of the 123-triazole core. c) Application of this reaction in the synthesis of the 1,2,3-triazolic core of Suvorexant.
Figure 22
The Palladium catalyzed C2’ ethoxy carbonylation of the 2-Aryl-1,2,3-triazole.
Figure 23
The Palladium catalyzed N2-Regioselective Arylation of β-Triazoyl Ribosides.
Figure 24
The copper catalyzed N2Arylation of substituted 1,2,3-triazoles.
Figure 25
Data on the yield and regioselectivity of different class of ligands for the copper catalyzed N2-Regioselective arylation of 1,2,3-triazoles.
Figure 26
Scope on the Copper catalyzed N2-Regioselective arylation of 1,2,3-triazoles.