Results 321 to 330 of about 2,937,461 (378)
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Syntheses based on nitrile oxides
Russian Chemical Bulletin, 1993Interaction of aromatic nitrile oxides with bis-trimethylsilylthiodiimide results in 2-amino-4-aryl-1,2,3,5-oxathiadiazoles, the first representatives of a new class of heterocyclic compounds.
Natalia V. Obruchnikova+4 more
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Cycloadditions of nitrile oxides with benzofurazan N-oxides
Journal of the Chemical Society, Perkin Transactions 1, 1990AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
N. G. Argyropoulos, John K. Gallos
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Syntheses based on nitrile oxides. 1. Reaction of aromatic nitrile oxides with N-cyanimides
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 1990The reaction of trialkylaminocyanimides with aromatic nitrile oxides leads to trialkylamino-(3-aryl-1,2,4-oxadiazol-5-yl)imides, while the corresponding reactions with sulfylcyanimines and phosphincyanimides do not take place. Using x-ray structural analysis the principal structural features of the 1,2,4-oxadiazole products have been elucidated.
Vladimir A. Ogurtsov+5 more
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The nitrile oxide–isocyanate rearrangement
J. Chem. Soc., Perkin Trans. 1, 1985The thermal rearrangement of 2,4,6-trimethylbenzonitrile N-oxide to the corresponding isocyanate has been investigated by double isotopic (2H and 18O) labelling and kinetic experiments. Rearrangement proceeds with exchange of oxygen atoms, and this exchange occurs exclusively between nitrile oxide molecules.
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, 2013
This article reports a new one-pot method for polymer preparation, which involves double click chemistry. In one pot, two click reactions take place sequentially by adding the reactants step by step. The first click reaction is to produce the monomer for
Yan Li, Bin Cheng
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This article reports a new one-pot method for polymer preparation, which involves double click chemistry. In one pot, two click reactions take place sequentially by adding the reactants step by step. The first click reaction is to produce the monomer for
Yan Li, Bin Cheng
semanticscholar +1 more source
ChemInform Abstract: Oxidation of Oximes to Nitrile Oxides with Hypervalent Iodine Reagents.
ChemInform, 2009AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Brian A. Mendelson+5 more
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, 2013
Masked o-benzoquinones, on reaction with nitrile oxides generated in situ from the corresponding hydroxamoyl chlorides, provide [3+2] cycloaddition products or novel isoxazoline derivatives through an unprecedented rearrangement.
Santhosh Kumar Chittimalla+3 more
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Masked o-benzoquinones, on reaction with nitrile oxides generated in situ from the corresponding hydroxamoyl chlorides, provide [3+2] cycloaddition products or novel isoxazoline derivatives through an unprecedented rearrangement.
Santhosh Kumar Chittimalla+3 more
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Nitrile Oxides, Sulfides, and Selenides
ChemInform, 2005AbstractFor Abstract see ChemInform Abstract in Full Text.
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ChemInform Abstract: New Aspects of Nitrile Oxides Chemistry.
ChemInform, 1993AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
AURICCHIO, SERGIO+3 more
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ChemInform Abstract: CATALYZED REARRANGEMENT OF NITRILE OXIDES INTO ISOCYANATES
Chemischer Informationsdienst, 1977The simultaneous migration of two ligands makes the rearrangement of nitrile oxides (1) to isocyanates (2) one of the most interesting ones in organic chemistry. However, use of the thermal reaction (1) is severely limited by competing dimerization. The rearrangement proceeds in excellent yields with SO2 as catalyst. equation image
Herbert Meier, Georg Trickes
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