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- Soai_reaction abstract "In organic chemistry, the Soai reaction is the alkylation of pyrimidine-5-carbaldehyde with diisopropylzinc. The reaction is autocatalytic and leads to rapidly increasing amounts of the same enantiomer of the product. The product pyrimidyl alcohol is chiral and induces that same chirality in further catalytic cycles. Starting with a low enantiomeric excess produces a product with very high enantiomeric excess. The reaction has been studied for clues about the origin of homochirality among certain classes of biomolecules.500pxThe Japanese chemist Kenso Soai (1950–) discovered the reaction in 1995. For his work in \"elucidating the origins of chirality and homochirality\", Soai received the Chemical Society of Japan award in 2010.Other chiral additives can be used as the initial source of asymmetric induction, with the major product of that first reaction being rapidly amplified.500px".
- Soai_reaction thumbnail Soai_autocatalysis.png?width=300.
- Soai_reaction wikiPageExternalLink 3402062.pdf.
- Soai_reaction wikiPageID "30993329".
- Soai_reaction wikiPageLength "4002".
- Soai_reaction wikiPageOutDegree "16".
- Soai_reaction wikiPageRevisionID "656384235".
- Soai_reaction wikiPageWikiLink Alkylation.
- Soai_reaction wikiPageWikiLink Asymmetric_induction.
- Soai_reaction wikiPageWikiLink Autocatalysis.
- Soai_reaction wikiPageWikiLink Biomolecule.
- Soai_reaction wikiPageWikiLink Category:Catalysis.
- Soai_reaction wikiPageWikiLink Category:Name_reactions.
- Soai_reaction wikiPageWikiLink Category:Organic_reactions.
- Soai_reaction wikiPageWikiLink Category:Stereochemistry.
- Soai_reaction wikiPageWikiLink Chemical_Society_of_Japan.
- Soai_reaction wikiPageWikiLink Diisopropylzinc.
- Soai_reaction wikiPageWikiLink Enantiomer.
- Soai_reaction wikiPageWikiLink Enantiomeric_excess.
- Soai_reaction wikiPageWikiLink Homochirality.
- Soai_reaction wikiPageWikiLink Kenso_Soai.
- Soai_reaction wikiPageWikiLink File:Cryptochirality_autocatalysis.png.
- Soai_reaction wikiPageWikiLink File:Soai_autocatalysis.png.
- Soai_reaction wikiPageWikiLinkText "Soai reaction".
- Soai_reaction wikiPageUsesTemplate Template:Chem-stub.
- Soai_reaction wikiPageUsesTemplate Template:Cite_journal.
- Soai_reaction wikiPageUsesTemplate Template:Cite_web.
- Soai_reaction wikiPageUsesTemplate Template:Reflist.
- Soai_reaction subject Category:Catalysis.
- Soai_reaction subject Category:Name_reactions.
- Soai_reaction subject Category:Organic_reactions.
- Soai_reaction subject Category:Stereochemistry.
- Soai_reaction hypernym Alkylation.
- Soai_reaction type Eponym.
- Soai_reaction type Process.
- Soai_reaction type Reaction.
- Soai_reaction comment "In organic chemistry, the Soai reaction is the alkylation of pyrimidine-5-carbaldehyde with diisopropylzinc. The reaction is autocatalytic and leads to rapidly increasing amounts of the same enantiomer of the product. The product pyrimidyl alcohol is chiral and induces that same chirality in further catalytic cycles. Starting with a low enantiomeric excess produces a product with very high enantiomeric excess.".
- Soai_reaction label "Soai reaction".
- Soai_reaction sameAs Q7549742.
- Soai_reaction sameAs Soai-Reaktion.
- Soai_reaction sameAs Soai-reactie.
- Soai_reaction sameAs m.0gg7tqp.
- Soai_reaction sameAs Q7549742.
- Soai_reaction wasDerivedFrom Soai_reaction?oldid=656384235.
- Soai_reaction depiction Soai_autocatalysis.png.
- Soai_reaction isPrimaryTopicOf Soai_reaction.