138801-86-2Relevant academic research and scientific papers
Searching for novel reusable biomass-derived solvents: Furfuryl alcohol/water azeotrope as a medium for waste-minimised copper-catalysed azide-alkyne cycloaddition
Rasina, Dace,Lombi, Aurora,Santoro, Stefano,Ferlin, Francesco,Vaccaro, Luigi
supporting information, p. 6380 - 6386 (2017/09/25)
Herein, we report the first application of the furfuryl alcohol/water azeotrope as a sustainable and easily recoverable reaction medium in organic chemistry. The applicability of this novel medium was tested in copper-catalysed azide-alkyne cycloaddition
Hydrogenations at room temperature and atmospheric pressure with mesoionic carbene-stabilized borenium catalysts
Eisenberger, Patrick,Bestvater, Brian P.,Keske, Eric C.,Crudden, Cathleen M.
supporting information, p. 2467 - 2471 (2015/02/19)
1,2,3-Triazolylidene-based mesoionic carbene boranes have been synthesized in a convenient one-pot protocol from the corresponding 1,2,3-triazolium salts, base, and borane. Borenium ions are obtained by hydride abstraction and serve as catalysts in mild hydrogenation reactions of imines and unsaturated N-heterocycles at ambient pressure and temperature.
High pressure assisted 1,3-dipolar cycloadditions: Formation of 1,2,3-triazoles from aryl azides and (trimethylsilyl)acetylene
Melai, Valeria,Brillante, Aldo,Zanirato, Paolo
, p. 2447 - 2449 (2007/10/03)
The cycloaddition of aryl azides to the corresponding 1,2,3-triazoles has been studied by means of FTIR spectroscopy in a diamond anvil cell at pressures up to 1 GPa. The rate of reaction increases logarithmically with pressure and the yield is close to q
Reactivity of Aryl and Heteroaryl Azides with Vinylsilane and Alkynylsilane. Formation of C-Silylated 1,2,3-Triazolines and 1,2,3-Triazoles
Zanirato, Paolo
, p. 2789 - 2796 (2007/10/02)
The reactions of the silylated dipolarophiles trimethyl(vinyl)silane, trimethoxy(vinyl)silane and (trimethylsilyl)acetylene, with some para-substituted phenyl azides, 2-azidobenzothiophene (2-BTA) and 3-azidobenzothiophene (3-BTA) have been examined.At room temperature these reactions give the respective 1-substituted 4-silylated-1,2,3-triazoline.However, only the reactions of 4-nitrophenyl and 4-cyanophenyl azide occur smoothly, furnishing triazolines in high yields; similar reactions with phenyl, 4-tolyl, 4-methoxyphenyl and 4-chlorophenyl azide are slower, affording mixtures of a 3-(N-arylamino)methyl-3,5-bis(trimethylsilyl)-1-p yrazoline, arising from the primary triazoline adduct through ring-opening to diazo compounds 2, and the corresponding 1-aryl-2-(trimethylsilyl)aziridine, resulting from nitrogen extrusion from the same elusive triazoline.On the other hand reactions of 2-BTA and 3-BTA involve rapid extrusion of nitrogen to afford exclusively the corresponding 1-(benzothienyl)-2-silylated aziridine.Results suggest that all these azides generally undergo 1,3-dipolar cycloadditions to terminally silylated alkenes to give triazoline adducts with the same geometrical orientation and whose thermal behaviour was found to be strongly dependent on the activating or deactivating effects exerted by N-1-substituents.Suitable support for electronic and steric factors acting in the same direction in the orientations of the former cyclo-aNAE adducts has been provided by the observation that the same aryl azides, 2-BTA and 3-BTA exhibit analogous 1,3-dipolar cycloadditions with (trimethylsilyl)acetylene from which stable 1-aryl(or heteroaryl)-4-trimethylsilyl-1,2,3-triazoles are obtained in quantitative yields.
