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- Steglich_esterification abstract "The Steglich esterification is a variation of an esterfication with dicyclohexylcarbodiimide as a coupling reagent and 4-dimethylaminopyridine as a catalyst. The reaction was first described by Wolfgang Steglich in 1978. It is an adaptation of an older method for the formation of amides by means of DCC (dicyclohexylcarbodiimide) and 1-hydroxybenzotriazole (HOBT). This reaction generally takes place at room temperature. A suitable solvent is dichloromethane. Because the reaction is mild, esters can be obtained that are inaccessible through other methods for instance esters of the sensitive 1,4-dihydroxybenzoic acid. A characteristic is the formal uptake of water generated in the reaction by DCC, forming the urea compound dicyclohexylurea (DCU).".
- Steglich_esterification thumbnail SteglichVeresterung_Uebersicht.svg?width=300.
- Steglich_esterification wikiPageExternalLink steglich-veresterung.htm.
- Steglich_esterification wikiPageID "22553448".
- Steglich_esterification wikiPageRevisionID "572341990".
- Steglich_esterification author "B. Neises and W. Steglich".
- Steglich_esterification collvol "7".
- Steglich_esterification collvolpages "93".
- Steglich_esterification hasPhotoCollection Steglich_esterification.
- Steglich_esterification prep "cv7p0093".
- Steglich_esterification title "Esterification of Carboxylic Acids with Dicyclohexylcarbodiimide/4-Dimethylaminopyridine: tert-Butyl ethyl fumarate".
- Steglich_esterification subject Category:Name_reactions.
- Steglich_esterification type ChemicalProcess113446390.
- Steglich_esterification type ChemicalReaction113447361.
- Steglich_esterification type NameReactions.
- Steglich_esterification type NaturalProcess113518963.
- Steglich_esterification type PhysicalEntity100001930.
- Steglich_esterification type Process100029677.
- Steglich_esterification comment "The Steglich esterification is a variation of an esterfication with dicyclohexylcarbodiimide as a coupling reagent and 4-dimethylaminopyridine as a catalyst. The reaction was first described by Wolfgang Steglich in 1978. It is an adaptation of an older method for the formation of amides by means of DCC (dicyclohexylcarbodiimide) and 1-hydroxybenzotriazole (HOBT). This reaction generally takes place at room temperature. A suitable solvent is dichloromethane.".
- Steglich_esterification label "Steglich esterification".
- Steglich_esterification label "Steglich-Veresterung".
- Steglich_esterification label "Steglich-verestering".
- Steglich_esterification label "Steglich酯化反应".
- Steglich_esterification sameAs Steglich-Veresterung.
- Steglich_esterification sameAs Steglich-verestering.
- Steglich_esterification sameAs m.05zl74x.
- Steglich_esterification sameAs Q695687.
- Steglich_esterification sameAs Q695687.
- Steglich_esterification sameAs Steglich_esterification.
- Steglich_esterification wasDerivedFrom Steglich_esterification?oldid=572341990.
- Steglich_esterification depiction SteglichVeresterung_Uebersicht.svg.
- Steglich_esterification isPrimaryTopicOf Steglich_esterification.