Results 211 to 220 of about 13,292 (250)
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Tetrahedron, 1970 
Abstract The role of structure in the reaction between enamines and nitroolefins has been evaluated. A synthetic method is presented for preparing substituted cyclic nitronic esters incorporating a 6-membered ring. Reaction of cyclopentanone, cyclohexanone and cycloheptanone enamines derived from pyrrolidine and morpholine with 2-nitro-1 ...
T.G. Archibald, A.T. Nielsen
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Abstract The role of structure in the reaction between enamines and nitroolefins has been evaluated. A synthetic method is presented for preparing substituted cyclic nitronic esters incorporating a 6-membered ring. Reaction of cyclopentanone, cyclohexanone and cycloheptanone enamines derived from pyrrolidine and morpholine with 2-nitro-1 ...
T.G. Archibald, A.T. Nielsen
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A Protocol To Transform Sulfones into Nitrones and Aldehydes.
Organic Letters, 2018A simple method to transform sulfones into nitrones and therefore into the corresponding carbonyl derivatives has been developed. Some examples demonstrate that it is a new reliable and versatile reaction in the toolbox of sulfones that has great ...
Eduardo Rodrigo, I. Alonso, M. Cid
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Nitrones and Cyclic Analogues [PDF]
AbstractFor Abstract see ChemInform Abstract in Full Text.
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Chemische Berichte, 1957 
AbstractDie Einwirkung von p‐Nitroso‐dialkylanilin auf 2‐ und 4‐Picolin‐jodmethylat ist grundsätzlich verschieden von der Nitron‐Bildung aus N‐Methylen‐pyridini‐umsalzen. Sie führt, wie eine einfache Methode der Abtrennung von Nitronen in Anil/Nitron‐Gemischen zeigt, überwiegend zu Anilen, auch wenn man die Nitron‐Bildung begünstigt.
Fritz Kröhnke +2 more
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AbstractDie Einwirkung von p‐Nitroso‐dialkylanilin auf 2‐ und 4‐Picolin‐jodmethylat ist grundsätzlich verschieden von der Nitron‐Bildung aus N‐Methylen‐pyridini‐umsalzen. Sie führt, wie eine einfache Methode der Abtrennung von Nitronen in Anil/Nitron‐Gemischen zeigt, überwiegend zu Anilen, auch wenn man die Nitron‐Bildung begünstigt.
Fritz Kröhnke +2 more
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Nitrone cycloadditions. regiochemistry.
Tetrahedron Letters, 1979Abstract The regiochemistry of nitrone cycloadditions has been reexamined. Certain nitrones afford regioisomeric mixtures of isoxazolidines, with a tendency toward increasing amounts of the 4-substituted regioisomer as the ionization potential of the dipolarophile is increased.
Joseph J. Tufariello +4 more
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Chemistry - An Asian Journal, 2018 
Highly enantioselective [3+2] cycloaddition of ynones and nitrones has been developed. Very bulky ligand, DTBM-SEGPHOS, was used for an effective asymmetric induction over distal reaction centers on the linear ynone dipolarophile and for prevention of ...
K. Honda, K. Mikami
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Highly enantioselective [3+2] cycloaddition of ynones and nitrones has been developed. Very bulky ligand, DTBM-SEGPHOS, was used for an effective asymmetric induction over distal reaction centers on the linear ynone dipolarophile and for prevention of ...
K. Honda, K. Mikami
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Studies on gold–nitrone systems
Dalton Transactions, 2019The dual reactivity of gold-nitrone systems was studied. A series of novel Au(i)–nitrone complexes with specific catalytic properties were prepared.
Helgi Freyr Jónsson, Anne Fiksdahl
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The periodate oxidation of nitrones
Journal of the Chemical Society C: Organic, 1966The periodate oxidation of some Δ1-pyrroline 1-oxides with two substituents at C-5 but unsubstituted at C-2 leads to a series of 4-nitrosopentanoic acids. Evidence is adduced for the course of the reaction. An N-alkylhydroxyamino-compound is oxidised in chloroform to the nitroso-compound by tetraethylammonium periodate, a potentially useful reagent ...
A. K. Qureshi, B. Sklarz
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Paired Electrosynthesis of a Nitrone
Chemistry Letters, 1997Abstract Dibutyl N-hydroxylamine was oxidized by WO42−/WO52−/ and BR−/Br2 redox mediators at cathode and anode, respectively. The corresponding nitrone, N-butylidenebutylamine N-oxide, was prepared at the both electrodes in divided and undivided cells. The paired electrosynthesis of the nitrone could be realized with current efficiencies
Tsutomu Nonaka, Wei Li
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