- dipolarophile
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Any compound (most often alkenes) that react with 1,3-dipoles in a cycloaddition reaction
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dipolarophile
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Nitrone-olefin 3+2 cycloaddition — The correct title of this article is Nitrone olefin [3+2] cycloaddition. The substitution or omission of any < > [ ] { } is due to technical restrictions. The nitrone olefin [3+2] cycloaddition reaction is the combination of a nitrone with… … Wikipedia
1,3-Dipolar cycloaddition — The 1,3 dipolar cycloaddition, also known as the Huisgen cycloaddition or Huisgen reaction, [1][2] is an organic chemical reaction belonging to the larger class of concerted, pericyclic cycloadditions. It is the reaction between a 1,3 dipole and… … Wikipedia
Diazoalkane 1,3-dipolar cycloaddition — The Diazoalkane 1,3 dipolar cycloaddition is a 1,3 dipolar cycloaddition (an organic reaction) between a 1,3 dipole diazo compound (notably diazomethane) and a dipolarophile. When the dipolarphile is an alkene, the reaction product is a… … Wikipedia
Prato reaction — The Prato reaction in fullerene chemistry describes the functionalization of fullerenes and nanotubes with azomethine ylides in a 1,3 dipolar cycloaddition. [cite journal | author = M. Maggini, G. Scorrano and M. Prato | title = Addition of… … Wikipedia
On water reaction — On water reactions are a group of organic reactions that take place as an emulsion in water and that exhibit an unusual reaction rate acceleration compared to the same reaction in an organic solvent or compared to the corresponding dry media… … Wikipedia
Aziridine — Chembox new ImageFileL1 = Aziridine.png ImageSizeL1 = 100px ImageFileR1 = Aziridine3d.png ImageSzieR1 = 100px IUPACName = Aziridine OtherNames = Azacyclopropane, Ethylene imine Section1 = Chembox Identifiers CASNo = 151 56 4 PubChem = SMILES =… … Wikipedia
151-56-4 — Aziridine Aziridine Général … Wikipédia en Français
Aziridine — Général Nom IUPAC … Wikipédia en Français
C2H5N — Aziridine Aziridine Général … Wikipédia en Français
Nitrile ylide — Nitrile ylides also known as nitrilium ylides, or nitrilium methylides are generally reactive intermediates. [1] Usually, they cannot be isolated. However, a structure has been determined on a particularly stable nitrile ylide by X ray… … Wikipedia
