Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Julia_olefination> ?p ?o. }
Showing items 1 to 39 of
39
with 100 items per page.
- Julia_olefination abstract "The Julia olefination (also known as the Julia–Lythgoe olefination) is the chemical reaction of phenyl sulfones (1) with aldehydes (or ketones) to give alkenes (3) after alcohol functionalization and reductive elimination using sodium amalgam or SmI2. The reaction is named after the French chemist Marc Julia.This transformation highly favors formation of the trans-alkene.All four steps can be carried out in a single reaction vessel, and use of R3X is optional. However, purification of the sulfone intermediate 2 leads to higher yield and purity. Most often R3 is acetyl or benzoyl, with acetic anhydride or benzoyl chloride used in the preparation of 2.Several reviews have been published.".
- Julia_olefination thumbnail Juila_Olefination_Scheme.png?width=300.
- Julia_olefination wikiPageExternalLink b208078h.
- Julia_olefination wikiPageID "4947978".
- Julia_olefination wikiPageRevisionID "600389093".
- Julia_olefination hasPhotoCollection Julia_olefination.
- Julia_olefination subject Category:Addition_reactions.
- Julia_olefination subject Category:Carbon-carbon_bond_forming_reactions.
- Julia_olefination subject Category:Free_radical_reactions.
- Julia_olefination subject Category:Name_reactions.
- Julia_olefination type AdditionReaction113427356.
- Julia_olefination type AdditionReactions.
- Julia_olefination type ChemicalProcess113446390.
- Julia_olefination type ChemicalReaction113447361.
- Julia_olefination type FreeRadicalReactions.
- Julia_olefination type NameReactions.
- Julia_olefination type NaturalProcess113518963.
- Julia_olefination type PhysicalEntity100001930.
- Julia_olefination type Process100029677.
- Julia_olefination comment "The Julia olefination (also known as the Julia–Lythgoe olefination) is the chemical reaction of phenyl sulfones (1) with aldehydes (or ketones) to give alkenes (3) after alcohol functionalization and reductive elimination using sodium amalgam or SmI2. The reaction is named after the French chemist Marc Julia.This transformation highly favors formation of the trans-alkene.All four steps can be carried out in a single reaction vessel, and use of R3X is optional.".
- Julia_olefination label "Julia olefination".
- Julia_olefination label "Julia-Olefinierung".
- Julia_olefination label "Julia-olefinering".
- Julia_olefination label "Olefinazione di Julia".
- Julia_olefination label "Oléfination de Julia".
- Julia_olefination label "ジュリア・リスゴーオレフィン化".
- Julia_olefination label "朱利亚烯烃合成".
- Julia_olefination sameAs Julia-Olefinierung.
- Julia_olefination sameAs Oléfination_de_Julia.
- Julia_olefination sameAs Olefinazione_di_Julia.
- Julia_olefination sameAs ジュリア・リスゴーオレフィン化.
- Julia_olefination sameAs Julia-olefinering.
- Julia_olefination sameAs m.0cwm04.
- Julia_olefination sameAs Q902237.
- Julia_olefination sameAs Q902237.
- Julia_olefination sameAs Julia_olefination.
- Julia_olefination wasDerivedFrom Julia_olefination?oldid=600389093.
- Julia_olefination depiction Juila_Olefination_Scheme.png.
- Julia_olefination isPrimaryTopicOf Julia_olefination.
