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- Eschenmoser_sulfide_contraction abstract "The Eschenmoser sulfide contraction is an organic reaction first described by Albert Eschenmoser for the synthesis of 1,3-dicarbonyl compounds from a thioester. The method requires a base and a tertiary phosphine. The method is of some relevance to organic chemistry and has been notably applied in the vitamin B12 total synthesis. Eschenmoser sulfur contraction.svgA base abstracts the labile hydrogen atom in the thioester, a sulfide anion is formed through an episulfide intermediate which is removed by the phosphine.Eschenmoser sulfur contraction mechanism↑ ↑ ↑ ↑".
- Eschenmoser_sulfide_contraction thumbnail Eschenmoser_sulfur_contraction.svg?width=300.
- Eschenmoser_sulfide_contraction wikiPageID "28281258".
- Eschenmoser_sulfide_contraction wikiPageLength "3382".
- Eschenmoser_sulfide_contraction wikiPageOutDegree "15".
- Eschenmoser_sulfide_contraction wikiPageRevisionID "532330708".
- Eschenmoser_sulfide_contraction wikiPageWikiLink Albert_Eschenmoser.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Carbapenem.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Carbonyl.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Category:Name_reactions.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Category:Organic_reactions.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Cocaine.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Episulfide.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Organic_chemistry.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Organic_reaction.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Thioester.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Total_synthesis.
- Eschenmoser_sulfide_contraction wikiPageWikiLink Vitamin_B12_total_synthesis.
- Eschenmoser_sulfide_contraction wikiPageWikiLink File:Eschenmoser_sulfur_contraction.svg.
- Eschenmoser_sulfide_contraction wikiPageWikiLink File:Eschenmoser_sulfur_contraction_mechanism.svg.
- Eschenmoser_sulfide_contraction wikiPageWikiLink File:Eschenmoser_sulfur_contraction_sakurai_1994.svg.
- Eschenmoser_sulfide_contraction wikiPageWikiLinkText "Eschenmoser sulfide contraction".
- Eschenmoser_sulfide_contraction wikiPageWikiLinkText "sulfur contraction".
- Eschenmoser_sulfide_contraction wikiPageUsesTemplate Template:Reflist.
- Eschenmoser_sulfide_contraction subject Category:Name_reactions.
- Eschenmoser_sulfide_contraction subject Category:Organic_reactions.
- Eschenmoser_sulfide_contraction hypernym Reaction.
- Eschenmoser_sulfide_contraction type Disease.
- Eschenmoser_sulfide_contraction type Eponym.
- Eschenmoser_sulfide_contraction type Reaction.
- Eschenmoser_sulfide_contraction comment "The Eschenmoser sulfide contraction is an organic reaction first described by Albert Eschenmoser for the synthesis of 1,3-dicarbonyl compounds from a thioester. The method requires a base and a tertiary phosphine. The method is of some relevance to organic chemistry and has been notably applied in the vitamin B12 total synthesis.".
- Eschenmoser_sulfide_contraction label "Eschenmoser sulfide contraction".
- Eschenmoser_sulfide_contraction sameAs Q5397185.
- Eschenmoser_sulfide_contraction sameAs m.0cnzwz2.
- Eschenmoser_sulfide_contraction sameAs Q5397185.
- Eschenmoser_sulfide_contraction wasDerivedFrom Eschenmoser_sulfide_contraction?oldid=532330708.
- Eschenmoser_sulfide_contraction depiction Eschenmoser_sulfur_contraction.svg.
- Eschenmoser_sulfide_contraction isPrimaryTopicOf Eschenmoser_sulfide_contraction.