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- Burgess_reagent abstract "The Burgess reagent or methyl N-(triethylammoniumsulfonyl)carbamate was developed in the laboratory of Edward M. Burgess at Georgia Tech. It is a mild and selective dehydrating reagent often used in organic chemistry. It is used to convert secondary and tertiary alcohol with an adjacent proton into alkenes. Primary alcohols do not work well. The reagent is soluble in common organic solvents and alcohol dehydration takes place with syn elimination. The Burgess reagent is a carbamate and a so-called inner salt. A general mechanism is shown below.General Mechanism for the Burgess reagent.↑ ↑".
- Burgess_reagent iupacName "1-methoxy-N-triethylammoniosulfonyl-methanimidate".
- Burgess_reagent thumbnail Burgess.svg?width=300.
- Burgess_reagent wikiPageID "2470340".
- Burgess_reagent wikiPageRevisionID "541698465".
- Burgess_reagent hasPhotoCollection Burgess_reagent.
- Burgess_reagent imagefile "Burgess.svg".
- Burgess_reagent iupacname "1".
- Burgess_reagent subject Category:Carbamates.
- Burgess_reagent subject Category:Quaternary_ammonium_compounds.
- Burgess_reagent subject Category:Reagents_for_organic_chemistry.
- Burgess_reagent type Abstraction100002137.
- Burgess_reagent type Carbamate114792281.
- Burgess_reagent type Carbamates.
- Burgess_reagent type Chemical114806838.
- Burgess_reagent type Compound114818238.
- Burgess_reagent type Material114580897.
- Burgess_reagent type Matter100020827.
- Burgess_reagent type OrganicCompound114727670.
- Burgess_reagent type Part113809207.
- Burgess_reagent type PhysicalEntity100001930.
- Burgess_reagent type QuaternaryAmmoniumCompound114691231.
- Burgess_reagent type QuaternaryAmmoniumCompounds.
- Burgess_reagent type Relation100031921.
- Burgess_reagent type Salt115010703.
- Burgess_reagent type Substance100019613.
- Burgess_reagent type ChemicalCompound.
- Burgess_reagent type ChemicalSubstance.
- Burgess_reagent type ChemicalSubstanceType.
- Burgess_reagent type ChemicalObject.
- Burgess_reagent type Thing.
- Burgess_reagent comment "The Burgess reagent or methyl N-(triethylammoniumsulfonyl)carbamate was developed in the laboratory of Edward M. Burgess at Georgia Tech. It is a mild and selective dehydrating reagent often used in organic chemistry. It is used to convert secondary and tertiary alcohol with an adjacent proton into alkenes. Primary alcohols do not work well. The reagent is soluble in common organic solvents and alcohol dehydration takes place with syn elimination.".
- Burgess_reagent label "Burgess reagent".
- Burgess_reagent label "Burgess-Reagenz".
- Burgess_reagent label "バージェス試薬".
- Burgess_reagent label "伯吉斯试剂".
- Burgess_reagent sameAs Burgess-Reagenz.
- Burgess_reagent sameAs バージェス試薬.
- Burgess_reagent sameAs m.07g99d.
- Burgess_reagent sameAs Q410969.
- Burgess_reagent sameAs Q410969.
- Burgess_reagent sameAs Burgess_reagent.
- Burgess_reagent wasDerivedFrom Burgess_reagent?oldid=541698465.
- Burgess_reagent depiction Burgess.svg.
- Burgess_reagent isPrimaryTopicOf Burgess_reagent.
