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ChemInform Abstract: 1,2,3‐TRIAZOLES

Chemischer Informationsdienst, 1974
AbstractIn einer Zusammenfassung wird die Synthese der verschiedenen 1,2,3‐Triazole aus Aziden mit Acetylenen oder aktivierten Methylenverbindungen und ausgehend von α‐Diketonen oder α‐Diketonderivaten er1äutert,und die Struktur, die physikalischen Eigenschaften sowie die chemischen Reaktionsweisen der Triazole bei Substitutionsreaktionen, Umwandlung ...
T. L. GILCHRIST, G. E. GYMER
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Synthesis of glucosylated 1,2,3-triazole derivatives

Carbohydrate Research, 1999
A series of potential bioactive compounds, 1-glucosyl-4-heterocyclyl-5-(p-substituted-phenyl)-1,2,3-triazoles , were synthesized. Highly stereoselective products were obtained in good yield. Primary activity screening showed that this type of N-glucosylic compound possessed antitumour and antiviral activities.
X M, Chen, Z J, Li, Z X, Ren, Z T, Huang
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Organocatalytic routes toward substituted 1,2,3-triazoles

Chemical Communications, 2015
The present feature article describes the different organocatalytic routes for the synthesis of substituted 1,2,3-triazoles.
Jubi, John, Joice, Thomas, Wim, Dehaen
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Synthesis of substituted septanosyl-1,2,3-triazoles

Carbohydrate Research, 2007
A carbohydrate-based oxepine, derived from 2-deoxy-D-arabino-hexopyranose, was used to prepare a family of septanosyl-1,2,3-triazoles in four steps. DMDO mediated epoxidation of the oxepine followed by trapping of the intermediate 1,2-anhydroseptanose by sodium azide gave the beta-substituted glycosyl azide. The septanosyl azide was then reacted with a
Steve, Castro   +3 more
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Glycidyl 4‐Functionalized‐1,2,3‐Triazole Polymers

Macromolecular Chemistry and Physics, 2012
AbstractA series of novel polymers, glycidyl 4‐functionalized 1,2,3‐triazole polymers (functionalized GTP) were synthesized by click functionalization of glycidyl azide polymer (GAP). Quantitative functionalization of the glycidyl polymer side groups was achieved due to the high reactivity of the azide–alkyne Huisgen cycloaddition under mild conditions.
Liu, D.   +5 more
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Structural basis of the impact sensitivities of 1-picryl-1,2,3-triazole, 2-picryl-1,2,3-triazole, 4-nitro-1-picryl-1,2,3-triazole, and 4-nitro-2-picryl-1,2,3-triazole

The Journal of Physical Chemistry, 1989
The isomeric pairs 1-picryl-1,2,3-triazole, 2-picryl-1,2,3-triazole and 4-nitro-1-picryl-1,2,3-triazole, 4-nitro-1-picryl-1,2,3-triazole differ dramatically in their impact sensitivity. Since these pairs of compounds have identical oxygen balance this strongly suggests that there is a difference in the decomposition mechanism.
C. B. Storm   +4 more
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From 1-Sulfonyl-4-aryl-1,2,3-triazoles to 1-Allenyl-5-aryl-1,2,3-triazoles

The Journal of Organic Chemistry, 2017
An efficient and highly regioselective synthesis of 1-allenyl-5-aryl-1,2,3-triazoles from 1-sulfonyl-4-aryl-1,2,3-triazoles is disclosed. 1-Sulfonyl-4-aryl-1,2,3-triazoles reacted with propargylic alcohols in the presence of trifluoroboron etherate to furnish 1-allenyl-5-aryl-1,2,3-triazoles.
Kai Huang   +3 more
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1,2,3-Triazol-carboxanilides and 1,2,3-triazol-(N-benzyl)-carboxamides as BK-potassium channel activators. XII

European Journal of Medicinal Chemistry, 2008
The chemical structures of many synthetic activators of large-conductance calcium-activated potassium channels (BK channels) satisfy a simple pharmacophore model, consisting of two appropriately substituted phenyl rings connected by a linker of a heterogeneous nature.
CALDERONE, VINCENZO   +6 more
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Titration characteristics of fluorous 1,2,3-triazol-4-ylmethyl ethers, bis(1,2,3-triazol-4-ylmethyl) ethers and bis(1,2,3-triazol-4-ylmethyl) amines

Journal of Fluorine Chemistry, 2016
Abstract The titration of a series of fluorous bis(1,2,3-triazol-4-ylmethyl) molecules with camphorsulfonic acid has been examined by 1 H NMR spectroscopy to investigate any conformational changes that might occur on protonation; it is envisaged that this information will assist in predicting their potential as ligands.
Dominic V. Francis   +2 more
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ChemInform Abstract: 1,2,3‐TRIAZOLES PART 2, 4‐AMINO‐5‐AMINOMETHYL‐1,2,3‐TRIAZOLES

Chemischer Informationsdienst, 1973
AbstractDurch Hydrolyse des Azomethins (I) wird das Aminocarbonitril (II) dargestellt; das Isomere (III) wird analog gewonnen.
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