Results 181 to 190 of about 11,801 (209)
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1,2,3-Triazoles. Part II. 4-Amino-5-aminomethyl-1,2,3-triazoles
Journal of the Chemical Society, Perkin Transactions 1, 19734-Amino-1-(and 2-)methyl-1,2,3-triazole-5-carbonitrile were made by acidic hydrolysis of 4-dimethylaminomethyleneamino-1-(and 2-)methyl-1,2,3-triazole-5-carbonitrile. These amino-nitriles, and also their known 3-methyl- and 3-benzyl-analogues, were hydrogenated to 4-amino-5-aminomethyl-1-methyl-1,2,3-triazole (1a) and its 2- and 3-methyl- and 3-benzyl ...
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Azolyl-substituted 1,2,3-triazoles
Russian Journal of Organic Chemistry, 2016Huisgen reaction of (E)-1,5-diarylpent-2-en-4-yn-1-ones and (E)-1,5-diarylpent-1-en-4-yn-3-ones afforded 1-aryl-3-(5-aryl-1H-1,2,3-triazol-4-yl)prop-2-en-1-ones and 3-aryl-1-(5-aryl-1H-1,2,3-triazol-4-yl)-prop-2-en-1-ones, respectively. (E)-1-Aryl-3-(5-phenyl-1H-1,2,3-triazol-4-yl)prop-2-en-1-ones reacted with hydrazine hydrate and phenylhydrazine to ...
A. A. Golovanov +7 more
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Fluorinated 1,2,3‐Triazoles: Terra Incognita in 1,2,3‐Triazoles Chemistry
ChemistrySelectAbstract This review is devoted to the synthesis and application of fluoro‐substituted 1,2,3‐triazoles. The analysis of the available studies of fluorinated triazoles indicates exceptional value properties especially for biomedical research, despite the significant limitations of synthetic methods of their preparation.
Nazariy Pokhodylo +2 more
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Aryl trifluoromethyl-1,2,3-triazoles
Journal of Fluorine Chemistry, 1991Abstract Diaryl-substituted trifluoromethyl-1,2,3-triazoles have been synthesized from aromaticazides and various substituted 1-aryl-3,3,3-trifluoro-1-propynes. The spectroscopic characteristicsof the products and the regioselectivity of the reaction are discussed. Animproved method for the synthesis of 1-aryl-3,3,3-trifluoro-1-propynes from 1-aryl-2-
G. Meazza, G. Zanardi
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Condensed 1,2,3-triazoles (review)
Chemistry of Heterocyclic Compounds, 2008Methods for the synthesis of condensed 1,2,3-triazoles, including mesoionic compounds, in the literature up to 2007 inclusively are presented. They are classified according to the method by which the molecular skeleton is formed. Mesoionic condensed compounds of the 1,2,3-triazole series are examined separately.
E. A. Shafran +3 more
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ChemInform Abstract: 1,2,3‐TRIAZOLES
Chemischer Informationsdienst, 1974AbstractIn 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, 1999A 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, 2015The 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, 2007A 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, 2012AbstractA 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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