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- Dihydroxylation abstract "Dihydroxylation is the process by which an alkene is converted into a vicinal diol. Although there are many routes to accomplish this oxidation, the most common and direct processes use a high-oxidation-state transition metal (typically osmium or manganese). The metal is often used as a catalyst, with some other stoichiometric oxidant present. In addition, other transition metals and non-transition metal methods have been developed and used to catalyze the reaction.".
- Dihydroxylation thumbnail Dihydroxylation.png?width=300.
- Dihydroxylation wikiPageID "3024813".
- Dihydroxylation wikiPageLength "15029".
- Dihydroxylation wikiPageOutDegree "33".
- Dihydroxylation wikiPageRevisionID "670220114".
- Dihydroxylation wikiPageWikiLink Alkene.
- Dihydroxylation wikiPageWikiLink Catalysis.
- Dihydroxylation wikiPageWikiLink Catalyst.
- Dihydroxylation wikiPageWikiLink Category:Alkenes.
- Dihydroxylation wikiPageWikiLink Category:Chemical_processes.
- Dihydroxylation wikiPageWikiLink Category:Diols.
- Dihydroxylation wikiPageWikiLink Dihydropyran.
- Dihydroxylation wikiPageWikiLink Diol.
- Dihydroxylation wikiPageWikiLink Gulose.
- Dihydroxylation wikiPageWikiLink Hydrolysis.
- Dihydroxylation wikiPageWikiLink Ligand.
- Dihydroxylation wikiPageWikiLink Mannose.
- Dihydroxylation wikiPageWikiLink Milas_hydroxylation.
- Dihydroxylation wikiPageWikiLink N-Methylmorpholine_N-oxide.
- Dihydroxylation wikiPageWikiLink Oxidation.
- Dihydroxylation wikiPageWikiLink Putrescine.
- Dihydroxylation wikiPageWikiLink Redox.
- Dihydroxylation wikiPageWikiLink Sharpless_asymmetric_dihydroxylation.
- Dihydroxylation wikiPageWikiLink Stoichiometric.
- Dihydroxylation wikiPageWikiLink Stoichiometry.
- Dihydroxylation wikiPageWikiLink Talose.
- Dihydroxylation wikiPageWikiLink Tetramethylenediamine.
- Dihydroxylation wikiPageWikiLink Transition_metal.
- Dihydroxylation wikiPageWikiLink Upjohn_dihydroxylation.
- Dihydroxylation wikiPageWikiLink Vicinal_(chemistry).
- Dihydroxylation wikiPageWikiLink File:Dihydroxylation.png.
- Dihydroxylation wikiPageWikiLink File:Hydroxylation_in_the_Synthesis_of_Brassinosteroid.png.
- Dihydroxylation wikiPageWikiLink File:NMO_vs_TMEDA.png.
- Dihydroxylation wikiPageWikiLink File:Osmium_Dihydroxylation_Mechanism.png.
- Dihydroxylation wikiPageWikiLink File:Prevost-Woodward_Modification.png.
- Dihydroxylation wikiPageWikiLink File:Prevost_Reaction.png.
- Dihydroxylation wikiPageWikiLink File:Prevost_and_Woodward_First_Steps.png.
- Dihydroxylation wikiPageWikiLink File:Prevost_and_Woodward_Scheme.png.
- Dihydroxylation wikiPageWikiLink File:Sharpless_Asymmetric_Dihydroxylation_Mnemonic.png.
- Dihydroxylation wikiPageWikiLink File:Sugar_synthesis.png.
- Dihydroxylation wikiPageWikiLink File:TMEDA_Transition_State.png.
- Dihydroxylation wikiPageWikiLink File:Woodward_Reaction.png.
- Dihydroxylation wikiPageWikiLinkText "Dihydroxylation".
- Dihydroxylation wikiPageWikiLinkText "dihydroxylation".
- Dihydroxylation hasPhotoCollection Dihydroxylation.
- Dihydroxylation wikiPageUsesTemplate Template:Reflist.
- Dihydroxylation subject Category:Alkenes.
- Dihydroxylation subject Category:Chemical_processes.
- Dihydroxylation subject Category:Diols.
- Dihydroxylation hypernym Process.
- Dihydroxylation type Election.
- Dihydroxylation comment "Dihydroxylation is the process by which an alkene is converted into a vicinal diol. Although there are many routes to accomplish this oxidation, the most common and direct processes use a high-oxidation-state transition metal (typically osmium or manganese). The metal is often used as a catalyst, with some other stoichiometric oxidant present. In addition, other transition metals and non-transition metal methods have been developed and used to catalyze the reaction.".
- Dihydroxylation label "Dihydroxylation".
- Dihydroxylation sameAs m.012cf216.
- Dihydroxylation sameAs Q19903952.
- Dihydroxylation sameAs Q19903952.
- Dihydroxylation wasDerivedFrom Dihydroxylation?oldid=670220114.
- Dihydroxylation depiction Dihydroxylation.png.
- Dihydroxylation isPrimaryTopicOf Dihydroxylation.