Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/1,3-Dipolar_cycloaddition> ?p ?o }
- 1,3-Dipolar_cycloaddition abstract "The 1,3-dipolar cycloaddition is a chemical reaction between a 1,3-dipole and a dipolarophile to form a five-membered ring. The earliest 1,3-dipolar cycloadditions were described in the late 19th century to the early 20th century, following the discovery of 1,3-dipoles. Mechanistic investigation and synthetic application were established in the 1960s, primarily through the work of Rolf Huisgen. Hence, the reaction is sometimes referred to as the Huisgen cycloaddition (this term is often used to specifically describe the 1,3-dipolar cycloaddition between an organic azide and an alkyne to generate 1,2,3-triazole). Currently, 1,3-dipolar cycloaddition is an important route to the regio- and stereoselective synthesis of five-membered heterocycles and their ring-opened acyclic derivatives.".
- 1,3-Dipolar_cycloaddition wikiPageID "1462065".
- 1,3-Dipolar_cycloaddition wikiPageLength "65341".
- 1,3-Dipolar_cycloaddition wikiPageOutDegree "259".
- 1,3-Dipolar_cycloaddition wikiPageRevisionID "677113737".
- 1,3-Dipolar_cycloaddition wikiPageWikiLink 1,2,3-Triazole.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink 1,2,3-triazole.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink 1,3-Dipolar_cycloaddition.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink 1,3-dipolar_cycloaddition.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink 1,3-dipole.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Acid_catalysis.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Activating_group.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Aldehyde.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Aldehydes.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Aldol_reaction.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Aliphatic_compound.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Alkene.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Alkenes.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Alkenyl.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Alkyne.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Alkynyl.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Allene.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Allyl.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Allyl_alcohol.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Antifungal_protein.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Aqueous_solution.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Aromatic_hydrocarbon.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Aromatization.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Atomic_orbital.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Azide.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Azide-alkyne_Huisgen_cycloaddition.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Aziridine.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Aziridines.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Azomethine_imine.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Azomethine_ylide.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Bicyclic_molecule.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Bioconjugation.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Bioorthogonal_chemistry.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Bond_dipole_moment.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Butyl.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Carbon_monoxide.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Carbon_nanotube.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Carbonyl.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Carbonyl_imine.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Carbonyl_oxide.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Carbonyl_ylide.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Carbonyls.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Carboxylic_acid.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Catalysis.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Catalyst.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Category:Cycloadditions.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Cell_(biology).
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Cell_membrane.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Chelation.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Chemical_reaction.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Chemical_synthesis.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Chemoselectivity.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Chiral.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Chiral_ligand.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Chirality.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Cis-trans_isomerism.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Cis–trans_isomerism.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Claisen_condensation.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Click_chemistry.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Concerted.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Concerted_reaction.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Conformational_isomerism.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Conjugate_variables_(thermodynamics).
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Copper.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Cycloaddition.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Cyclooctyne.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Cytotoxicity.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Deactivating_groups.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Decalin.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Delocalized_electron.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Dewar-Zimmerman_rules.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Diastereomer.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Diastereomeric.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Diastereoselectivity.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Diazo.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Diazoalkane.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Diazomethane.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Dibromocarbenes.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Dichlorocarbenes.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Diels-Alder_reaction.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Diels–Alder_reaction.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Dihydrofuran.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Dimethyl_sulfoxide.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Dipolarophile.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Electrocyclic_reaction.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Electronic_effect.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Electrophile.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Electrophilic_aromatic_directing_groups.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Elimination_reaction.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Enantiomer.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Enantioselective_synthesis.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Endo-exo_isomerism.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Enol.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Enolate.
- 1,3-Dipolar_cycloaddition wikiPageWikiLink Entropy_of_activation.