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by Wang, Z and Hong, W and Wang, H
ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES, ISSN 1433-7266, 09/2018, Volume 233, Issue 5, pp. 831 - 832
C18H16N4O5, triclinic, P (1) over bar (no. 2), a = 8.4076(6) angstrom, b = 8.6630(5) angstrom, c = 12.0763(8) angstrom, alpha = 102.046(3)degrees, beta =... 
1,2,3-TRIAZOLES | CRYSTALLOGRAPHY
Journal Article
1980, ISBN 9780471078272, Volume 39., ix, 349
Book
SYNTHESIS-STUTTGART, ISSN 0039-7881, 01/2017, Volume 49, Issue 1, pp. 29 - 41
Journal Article
Zeitschrift für Kristallographie - New Crystal Structures, ISSN 1433-7266, 11/2018, Volume 233, Issue 6, pp. 985 - 986
, orthorhombic, (no. 61), = 8.4167(7) Å, = 14.0370(10) Å, = 34.664(3) Å, = 4095.4(6) Å , = 8, ) = 0.0457, ) = 0.1001, = 150(2) K. 
1569462 | 1,2,3-TRIAZOLES | CRYSTALLOGRAPHY
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 05/2015, Volume 56, Issue 22, pp. 2853 - 2859
1,2,3-Triazoles find applications in several major technological areas, and especially in drug discovery. The click-chemistry approaches based on Huisgen’s... 
1,2,3-Triazoles | Amide isosters | Regioselectivity | Metal-free cycloaddition | Click-chemistry | AZIDE-ALKYNE CYCLOADDITION | ONE-POT | RUTHENIUM-CATALYZED CYCLOADDITION | SOLID-PHASE | CHEMISTRY, ORGANIC | 1,5-DISUBSTITUTED 1,2,3-TRIAZOLES | TERMINAL ALKYNES | IONIC LIQUID | METAL-FREE SYNTHESIS | 1,3-DIPOLAR CYCLOADDITION | CONTINUOUS-FLOW | Triazoles | Methods
Journal Article
Chemical Communications, ISSN 1359-7345, 07/2015, Volume 51, Issue 54, pp. 10797 - 10806
Journal Article
Chemical Communications, ISSN 1359-7345, 6/2015, Volume 51, Issue 54, pp. 1797 - 186
The present feature article describes the different organocatalytic routes for the synthesis of substituted 1,2,3-triazoles. This methodology has recently... 
Methodology | Triazoles | Synthesis
Journal Article
by Deng, XC and Lei, X and Nie, G and Jia, LH and Li, YX and Chen, YF
JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, 06/2017, Volume 82, Issue 12, pp. 6163 - 6171
An efficient copper-catalyzed C-N bond formation by N-H/C-H cross-dehydrogenative coupling (CDC) between NH-1,2,3-triazoles and N,N-dialkylamides has been... 
1,3-DIPOLAR CYCLOADDITION REACTION | H BOND ADJACENT | FACILE SYNTHESIS | COUPLING REACTION | EFFICIENT SYNTHESIS | REGIOSELECTIVE SYNTHESIS | CHEMISTRY, ORGANIC | 1,5-DISUBSTITUTED 1,2,3-TRIAZOLES | SUBSTITUTED 1,2,3-TRIAZOLES | METAL-FREE | POST-TRIAZOLE ARYLATION
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 04/2015, Volume 56, Issue 17, pp. 2145 - 2148
A convenient and efficient method for the synthesis of -2-aryl 1,2,3-triazoles from α-arylhydrazonoketones under copper-catalyzed oxidative conditions has been... 
1,2,3-Triazoles | Copper-catalyzed | Hydrazonoketones | Aerobic oxidative | N–N bond | N-N bond | CONVENIENT SYNTHESIS | ONE-POT SYNTHESIS | CLICK CHEMISTRY | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | 1,5-DISUBSTITUTED 1,2,3-TRIAZOLES | SUBSTITUTED 1,2,3-TRIAZOLES | N BOND-FORMATION | POST-TRIAZOLE ARYLATION | HIV-1 PROTEASE | MOLECULAR-OXYGEN
Journal Article
Zeitschrift für Kristallographie - New Crystal Structures, ISSN 1433-7266, 11/2017, Volume 232, Issue 6, pp. 979 - 980
, monoclinic, (no. 14), = 14.9289(7) Å, = 7.8070(4) Å, = 12.4664(7) Å, = 106.821(4)°, = 1390.79(13) Å , = 4, ) = 0.0646, ) = 0.1682, T = 293(2) K. 
1572566 | 1,2,3-TRIAZOLES | CRYSTALLOGRAPHY
Journal Article
Organic Letters, ISSN 1523-7060, 05/2003, Volume 5, Issue 11, pp. 1951 - 1954
[GRAPHIC] The construction of multivalent neoglycoconjugates is efficiently achieved by the regiospecific catalytic cycloaddition of alkynes and azides using... 
CHEMISTRY, ORGANIC | 1,3-DIPOLAR CYCLOADDITIONS | ARYL | 1,2,3-TRIAZOLES | GLYCOBIOLOGY
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 06/2017, Volume 58, Issue 23, pp. 2272 - 2275
The ruthenium assisted azide-alkyne cycloaddition (RuAAC) reaction is a well-established method for the generation of 1,5- and 1,4,5-substituted... 
Side-chain protected peptides | Ruthenium catalysts | Ruthenium-assisted azide-alkyne cycloaddition | 1,5-Substituted 1,2,3-triazoles | 1,4.5-Substituted 1,2,3-triazoles
Journal Article
Organic Letters, ISSN 1523-7060, 04/2017, Volume 19, Issue 8, pp. 2098 - 2101
Metalated triazoles are the key reactive intermediate of the current click reaction (CuAAC). Bench-stable 5-stannyl triazoles are obtained by a... 
ONE-POT REACTION | AZIDE-ALKYNE CYCLOADDITION | MEDIATED FLUORINATION | 1,4,5-SUBSTITUTED 1,2,3-TRIAZOLES | 1,4,5-TRISUBSTITUTED 1,2,3-TRIAZOLES | ARYL STANNANES | REGIOSELECTIVE SYNTHESIS | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | ORGANIC AZIDES | CATALYZED TRIFLUOROMETHYLTHIOLATION
Journal Article
Synthetic Communications, ISSN 0039-7911, 07/2017, Volume 47, Issue 13, pp. 1193 - 1200
1,2,3-Triazoles, significant five-membered ring N-heterocycles, are main structural moieties in well-designed materials, pharmaceutical agents, bioactive... 
1,2,3-Triazoles | metal-free synthesis | azide-free synthesis | 1,4-DISUBSTITUTED 1,2,3-TRIAZOLES | REGIOSPECIFIC SYNTHESIS | HUISGEN CYCLOADDITION | ONE-POT | TOSYLHYDRAZONES | CHEMISTRY, ORGANIC | 1,5-DISUBSTITUTED 1,2,3-TRIAZOLES | 1,3-DIPOLAR CYCLOADDITION | CONSTRUCTION | CHEMISTRY | ALKYNE CYCLOADDITION
Journal Article
Current Organic Synthesis, ISSN 1570-1794, 01/2014, Volume 11, Issue 5, pp. 647 - 675
Journal Article
Current Organic Chemistry, ISSN 1385-2728, 07/2016, Volume 20, Issue 15, pp. 1591 - 1647
Journal Article
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