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- Milas_hydroxylation abstract "The Milas hydroxylation is an organic reaction converting an alkene to a vicinal diol, and was developed by N. A. Milas in the 1930s. The cis-diol is formed by reaction of alkenes with hydrogen peroxide and either ultraviolet light or a catalytic osmium tetroxide, vanadium oxide, or chromium oxide.The reaction has been superseded in synthetic chemistry by the Upjohn dihydroxylation and later by the Sharpless asymmetric dihydroxylation.".
- Milas_hydroxylation thumbnail Milas_hydroxylation.png?width=300.
- Milas_hydroxylation wikiPageID "9995380".
- Milas_hydroxylation wikiPageLength "1809".
- Milas_hydroxylation wikiPageOutDegree "13".
- Milas_hydroxylation wikiPageRevisionID "689947572".
- Milas_hydroxylation wikiPageWikiLink Alkene.
- Milas_hydroxylation wikiPageWikiLink Category:Name_reactions.
- Milas_hydroxylation wikiPageWikiLink Category:Organic_redox_reactions.
- Milas_hydroxylation wikiPageWikiLink Chromium_oxide.
- Milas_hydroxylation wikiPageWikiLink Diol.
- Milas_hydroxylation wikiPageWikiLink Hydrogen_peroxide.
- Milas_hydroxylation wikiPageWikiLink Organic_reaction.
- Milas_hydroxylation wikiPageWikiLink Osmium_tetroxide.
- Milas_hydroxylation wikiPageWikiLink Sharpless_asymmetric_dihydroxylation.
- Milas_hydroxylation wikiPageWikiLink Upjohn_dihydroxylation.
- Milas_hydroxylation wikiPageWikiLink Vanadium_oxide.
- Milas_hydroxylation wikiPageWikiLink Vicinal_(chemistry).
- Milas_hydroxylation wikiPageWikiLink File:Milas_hydroxylation.png.
- Milas_hydroxylation wikiPageWikiLinkText "Milas hydroxylation".
- Milas_hydroxylation wikiPageUsesTemplate Template:Reaction-stub.
- Milas_hydroxylation wikiPageUsesTemplate Template:Reflist.
- Milas_hydroxylation subject Category:Name_reactions.
- Milas_hydroxylation subject Category:Organic_redox_reactions.
- Milas_hydroxylation hypernym Reaction.
- Milas_hydroxylation type Disease.
- Milas_hydroxylation type Eponym.
- Milas_hydroxylation type Reaction.
- Milas_hydroxylation comment "The Milas hydroxylation is an organic reaction converting an alkene to a vicinal diol, and was developed by N. A. Milas in the 1930s. The cis-diol is formed by reaction of alkenes with hydrogen peroxide and either ultraviolet light or a catalytic osmium tetroxide, vanadium oxide, or chromium oxide.The reaction has been superseded in synthetic chemistry by the Upjohn dihydroxylation and later by the Sharpless asymmetric dihydroxylation.".
- Milas_hydroxylation label "Milas hydroxylation".
- Milas_hydroxylation sameAs Q2137095.
- Milas_hydroxylation sameAs هدرجة_ميلاس.
- Milas_hydroxylation sameAs Hidroxilación_de_Milas.
- Milas_hydroxylation sameAs Milas-hydroxylering.
- Milas_hydroxylation sameAs m.02pz6gs.
- Milas_hydroxylation sameAs மிலாசு_ஐதராக்சிலேற்றம்.
- Milas_hydroxylation sameAs Q2137095.
- Milas_hydroxylation sameAs Milas双羟基化反应.
- Milas_hydroxylation wasDerivedFrom Milas_hydroxylation?oldid=689947572.
- Milas_hydroxylation depiction Milas_hydroxylation.png.
- Milas_hydroxylation isPrimaryTopicOf Milas_hydroxylation.