Results 311 to 320 of about 2,937,461 (378)
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anti-Diradical Formation in 1,3-Dipolar Cycloadditions of Nitrile Oxides to Acetylenes.
Journal of Organic Chemistry, 2015By means of high level quantum chemical calculations (B2PLYPD and CCSD(T)), the mechanisms of the reaction of nitrile oxides with alkenes and alkynes were investigated.
Gebhard Haberhauer+2 more
semanticscholar +1 more source
Fluorescent Probes from Stable Aromatic Nitrile Oxides
, 2016Stable aromatic nitrile oxides underwent a 1,3-dipolar cycloaddition reaction with 1-iodo-4-(prop-2-yn-1-yloxy)benzene to afford the expected isoxazoles in very good yields as single regioisomers.
Luigi Ferdinando Minuti+3 more
semanticscholar +1 more source
Journal of Organic Chemistry, 2014
A highly enantioselective 1,3-dipolar cycloaddition of nitrile oxides with 3-arylidene-oxindoles was realized by a chiral N,N'-dioxide-nickel(II) complex catalyst under mild reaction conditions.
Xiangjin Lian+5 more
semanticscholar +1 more source
A highly enantioselective 1,3-dipolar cycloaddition of nitrile oxides with 3-arylidene-oxindoles was realized by a chiral N,N'-dioxide-nickel(II) complex catalyst under mild reaction conditions.
Xiangjin Lian+5 more
semanticscholar +1 more source
Fragmentation of nitrile oxides with triethylamine
Tetrahedron Letters, 1983Abstract The formation of 1,2,4-oxadiazoles is frequently observed as a side reaction in cycl o additions with nitrile oxides generated in situ and follows from a fragmentation induced by Et3N. This latter is oxidized to N,N-diethylvinylamine, which is trapped as a cycloadduct.
A. Compagnini+3 more
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, 2014
A highly efficient and general protocol has been developed for the facile synthesis of highly diversified 1,3,5-trisubstituted pyrazoles and 3,5-disubstituted 2-isoxazolines through one-pot tandem intermolecular, as well as intramolecular, dipolar [3 + 2]
G. Pal, S. Paul, P. Ghosh, Asish R. Das
semanticscholar +1 more source
A highly efficient and general protocol has been developed for the facile synthesis of highly diversified 1,3,5-trisubstituted pyrazoles and 3,5-disubstituted 2-isoxazolines through one-pot tandem intermolecular, as well as intramolecular, dipolar [3 + 2]
G. Pal, S. Paul, P. Ghosh, Asish R. Das
semanticscholar +1 more source
Organic Letters, 2013
Hypervalent iodine catalyzed oxidation of aldoximes using oxone as a terminal oxidant generates nitrile oxides, which react with alkenes and alkynes to give the corresponding isoxazolines and isoxazoles in moderate to good yields.
A. Yoshimura+6 more
semanticscholar +1 more source
Hypervalent iodine catalyzed oxidation of aldoximes using oxone as a terminal oxidant generates nitrile oxides, which react with alkenes and alkynes to give the corresponding isoxazolines and isoxazoles in moderate to good yields.
A. Yoshimura+6 more
semanticscholar +1 more source
The addition of nitrile oxides to C60
Tetrahedron, 1996Abstract The 1,3-dipolar cycloaddition of nitrile oxides to C60 is described. These reactions result in the formation of fullerene-fused isoxazoline heterocycles bearing a series of different substituents in 3-position. The preparation and spectroscopic characterization of these compounds are reported, as well as some investigations of the reactivity
Mark S. Meier, Magdalena Poplawska
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, 2018
A new synthetic route for obtaining polyfunctional nitrile N-oxides from OH-tethering nitrile N-oxide is reported. OH-Tethering nitrile N-oxide is synthesized using the proposed route by using an intermediary nitroalkane and derived to polyfunctional ...
H. Sogawa+4 more
semanticscholar +1 more source
A new synthetic route for obtaining polyfunctional nitrile N-oxides from OH-tethering nitrile N-oxide is reported. OH-Tethering nitrile N-oxide is synthesized using the proposed route by using an intermediary nitroalkane and derived to polyfunctional ...
H. Sogawa+4 more
semanticscholar +1 more source
Chemical Communications, 2013
A short and flexible [3+2+1] synthetic strategy was developed for the synthesis of substituted tetrahydropyran-4-ones, featuring [3+2]-cycloaddition of α,β-unsaturated nitrile oxides and alkenes and oxa-Michael cyclization in a 6-endo-trig fashion.
Hongliang Yao+2 more
semanticscholar +1 more source
A short and flexible [3+2+1] synthetic strategy was developed for the synthesis of substituted tetrahydropyran-4-ones, featuring [3+2]-cycloaddition of α,β-unsaturated nitrile oxides and alkenes and oxa-Michael cyclization in a 6-endo-trig fashion.
Hongliang Yao+2 more
semanticscholar +1 more source
Nitrile Oxide Cycloadditions to Olefinated Sugars.
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Pedro A. Colinas+4 more
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