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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 through an intramolecular elimination reaction. The Burgess reagent is a carbamate and an 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 wikiPageLength "2613".
- Burgess_reagent wikiPageOutDegree "19".
- Burgess_reagent wikiPageRevisionID "676368509".
- Burgess_reagent wikiPageWikiLink Alcohol.
- Burgess_reagent wikiPageWikiLink Alkene.
- Burgess_reagent wikiPageWikiLink Carbamate.
- Burgess_reagent wikiPageWikiLink Category:Carbamates.
- Burgess_reagent wikiPageWikiLink Category:Dehydrating_agents.
- Burgess_reagent wikiPageWikiLink Category:Quaternary_ammonium_compounds.
- Burgess_reagent wikiPageWikiLink Category:Reagents_for_organic_chemistry.
- Burgess_reagent wikiPageWikiLink Category:Zwitterions.
- Burgess_reagent wikiPageWikiLink Chlorosulfonyl_isocyanate.
- Burgess_reagent wikiPageWikiLink Edward_M._Burgess.
- Burgess_reagent wikiPageWikiLink Ei_mechanism.
- Burgess_reagent wikiPageWikiLink Georgia_Institute_of_Technology.
- Burgess_reagent wikiPageWikiLink Methanol.
- Burgess_reagent wikiPageWikiLink Organic_chemistry.
- Burgess_reagent wikiPageWikiLink Syn_and_anti_addition.
- Burgess_reagent wikiPageWikiLink Triethylamine.
- Burgess_reagent wikiPageWikiLink Zwitterion.
- Burgess_reagent wikiPageWikiLink File:Burgess_mechanism.png.
- Burgess_reagent wikiPageWikiLink File:Burgessreagent.svg.
- Burgess_reagent wikiPageWikiLinkText "Burgess Reagent".
- Burgess_reagent wikiPageWikiLinkText "Burgess reagent".
- Burgess_reagent imagefile "Burgess.svg".
- Burgess_reagent iupacname "1".
- Burgess_reagent wikiPageUsesTemplate Template:Chembox.
- Burgess_reagent wikiPageUsesTemplate Template:Chembox_Hazards.
- Burgess_reagent wikiPageUsesTemplate Template:Chembox_Identifiers.
- Burgess_reagent wikiPageUsesTemplate Template:Chembox_Properties.
- Burgess_reagent wikiPageUsesTemplate Template:Reflist.
- Burgess_reagent subject Category:Carbamates.
- Burgess_reagent subject Category:Dehydrating_agents.
- Burgess_reagent subject Category:Quaternary_ammonium_compounds.
- Burgess_reagent subject Category:Reagents_for_organic_chemistry.
- Burgess_reagent subject Category:Zwitterions.
- Burgess_reagent type ChemicalCompound.
- Burgess_reagent type ChemicalSubstance.
- Burgess_reagent type Drug.
- Burgess_reagent type Amide.
- Burgess_reagent type Carbamate.
- Burgess_reagent type Ester.
- Burgess_reagent type Reagent.
- Burgess_reagent type ChemicalObject.
- Burgess_reagent type Thing.
- Burgess_reagent type Q11173.
- 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 through an intramolecular elimination reaction.".
- Burgess_reagent label "Burgess reagent".
- Burgess_reagent sameAs Q410969.
- Burgess_reagent sameAs Burgess-Reagenz.
- Burgess_reagent sameAs バージェス試薬.
- Burgess_reagent sameAs m.07g99d.
- Burgess_reagent sameAs Реактив_Бёрджесса.
- Burgess_reagent sameAs Burgesov_reagens.
- Burgess_reagent sameAs Burgesov_reagens.
- Burgess_reagent sameAs Q410969.
- Burgess_reagent sameAs 伯吉斯试剂.
- Burgess_reagent wasDerivedFrom Burgess_reagent?oldid=676368509.
- Burgess_reagent depiction Burgess.svg.
- Burgess_reagent isPrimaryTopicOf Burgess_reagent.