Results 1 to 10 of about 116,077 (356)
The demand to study the cellular localization of specific lipids has led to recent advances in lipid probes and microscopy. Alkyne lipids bear a small, noninterfering tag and can be detected upon click reaction with an azide-coupled reporter. Fluorescent
Anne Gaebler +3 more
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The emergence of bioorthogonal reactions has greatly broadened the scope of biomolecule labeling and detecting. Of all the bioorthogonal reactions that have been developed, the copper-catalyzed azide-alkyne cycloaddition (CuAAC) is the most widely ...
Li Li, Zhiyuan Zhang
semanticscholar +1 more source
Design, Synthesis and Characterization of Novel Isoxazole Tagged Indole Hybrid Compounds
Sixteen new isoxazole tagged indole compounds have been synthesized via copper (I) catalyzed click chemistry of the aryl hydroxamoyl chloride and an indole containing alkyne moiety. The chemical structure of the synthesized compounds has been established
Al-Qawasmeh Raed A. +6 more
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Polymer-Supported-Cobalt-Catalyzed Regioselective Cyclotrimerization of Aryl Alkynes [PDF]
Abhijit Sen +5 more
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The co-ordination of FcCCC6H4-4-NO2 (1) to a ruthenium carbonyl cluster to yield [Ru3(mu 3-FcCCC6H4-4-NO2) (mu-dppm)( mu-CO)(CO)7] (2) is reported. The cyclic voltammograms of these compounds and of the analogous clusters [Ru3(mu3 -eta2-C6 H5CCC6H4-4-R ...
Rosseto Renato +3 more
doaj
Total Synthesis of Chiral Falcarindiol Analogues Using BINOL-Promoted Alkyne Addition to Aldehydes
An enantioselective total synthesis of chiral falcarindiol analogues from buta-1,3-diyn-1-yltriisopropylsilane is reported. The key step in this synthesis is BINOL-promoted asymmetric diacetylene addition to aldehydes.
Li Wang +7 more
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Fluorohydration of alkynes via I(I)/I(III) catalysis
Substrate specificity is ubiquitous in biological catalysis, but less pervasive in the realm of small-molecule catalysis. Herein, we disclose an intriguing example of substrate specificity that was observed whilst exploring catalysis-based routes to ...
Jessica Neufeld +2 more
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Citation: 'alkynes' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.A00236 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms. Requests for commercial usage
openaire +1 more source
Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes [PDF]
Pradeep K. R. Panyam +6 more
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