Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Nitrile_ylide> ?p ?o }
Showing triples 1 to 40 of
40
with 100 triples per page.
- Nitrile_ylide abstract "Nitrile ylides also known as nitrilium ylides, or nitrilium methylides are generally reactive intermediates. With a few exceptions, they cannot be isolated. However, a structure has been determined on a particularly stable nitrile ylide by X-ray crystallography. Another nitrile ylide has been captured under cryogenic conditions.As ylides, they possess a negative charge and a positive charge on adjacent atoms. As a 1,3-dipole, several resonance structures can be drawn (1a-d). The most appropriate resonance structure is dependent upon the substituent pattern (the identity of the R and R' groups in 1 and 2). The 3-dimensional structure of the nitrilium ylide itself may also provide a clue as to the most appropriate resonance structure, with a linear R-C≡N-C unit supportive of the charge distribution indicated for resonance structures 1a & 1b and also consistent with the nomenclature nitrilium ylide. As resonance structures 1c & 1d become more important the nitrilium ylide distorts its geometry in favor of a different valence tautomer, 2.1024pxNitrile ylides are isoelectronic with nitrile oxides.124px".
- Nitrile_ylide thumbnail NitrileYlide_Res_VB_ST.svg?width=300.
- Nitrile_ylide wikiPageExternalLink 0101Viewer.html.
- Nitrile_ylide wikiPageID "26945417".
- Nitrile_ylide wikiPageLength "2971".
- Nitrile_ylide wikiPageOutDegree "18".
- Nitrile_ylide wikiPageRevisionID "612638957".
- Nitrile_ylide wikiPageWikiLink 1,3-Dipolar_cycloaddition.
- Nitrile_ylide wikiPageWikiLink 1,3-dipole.
- Nitrile_ylide wikiPageWikiLink Alkyne.
- Nitrile_ylide wikiPageWikiLink Azirine.
- Nitrile_ylide wikiPageWikiLink Carbene.
- Nitrile_ylide wikiPageWikiLink Category:Functional_groups.
- Nitrile_ylide wikiPageWikiLink Imine.
- Nitrile_ylide wikiPageWikiLink Isoxazole.
- Nitrile_ylide wikiPageWikiLink Methanol.
- Nitrile_ylide wikiPageWikiLink Nitrile.
- Nitrile_ylide wikiPageWikiLink Protonation.
- Nitrile_ylide wikiPageWikiLink Pyrroline.
- Nitrile_ylide wikiPageWikiLink Reactive_intermediate.
- Nitrile_ylide wikiPageWikiLink Tautomer.
- Nitrile_ylide wikiPageWikiLink X-ray_crystallography.
- Nitrile_ylide wikiPageWikiLink Ylide.
- Nitrile_ylide wikiPageWikiLink File:Nitrile-oxide-2D-B.png.
- Nitrile_ylide wikiPageWikiLink File:NitrileYlide_Res_VB_ST.svg.
- Nitrile_ylide wikiPageWikiLinkText "Nitrile ylide".
- Nitrile_ylide wikiPageWikiLinkText "nitrile ylide".
- Nitrile_ylide wikiPageUsesTemplate Template:Reflist.
- Nitrile_ylide subject Category:Functional_groups.
- Nitrile_ylide type Group.
- Nitrile_ylide type Group.
- Nitrile_ylide comment "Nitrile ylides also known as nitrilium ylides, or nitrilium methylides are generally reactive intermediates. With a few exceptions, they cannot be isolated. However, a structure has been determined on a particularly stable nitrile ylide by X-ray crystallography. Another nitrile ylide has been captured under cryogenic conditions.As ylides, they possess a negative charge and a positive charge on adjacent atoms. As a 1,3-dipole, several resonance structures can be drawn (1a-d).".
- Nitrile_ylide label "Nitrile ylide".
- Nitrile_ylide sameAs Q17130695.
- Nitrile_ylide sameAs m.0bmf5f8.
- Nitrile_ylide sameAs Нітриліліди.
- Nitrile_ylide sameAs Q17130695.
- Nitrile_ylide wasDerivedFrom Nitrile_ylide?oldid=612638957.
- Nitrile_ylide depiction NitrileYlide_Res_VB_ST.svg.
- Nitrile_ylide isPrimaryTopicOf Nitrile_ylide.