Benzylidene acetal (original) (raw)
In organic chemistry, a benzylidene acetal is the functional group with the structural formula C6H5CH(OR)2 (R = alkyl, aryl). Benzylidene acetals are used as protecting groups in glycochemistry. These compounds can also be oxidized to carboxylic acids in order to open important biological molecules, such as glycosaminoglycans, to other routes of synthesis. They arise from the reaction of a 1,2- or 1,3-diols with benzaldehyde. Other aromatic aldehydes are also used.
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| dbo:abstract | In organic chemistry, a benzylidene acetal is the functional group with the structural formula C6H5CH(OR)2 (R = alkyl, aryl). Benzylidene acetals are used as protecting groups in glycochemistry. These compounds can also be oxidized to carboxylic acids in order to open important biological molecules, such as glycosaminoglycans, to other routes of synthesis. They arise from the reaction of a 1,2- or 1,3-diols with benzaldehyde. Other aromatic aldehydes are also used. (en) Bensylidenacetal är inom organisk kemi en funktionell grupp med strukturformeln C6H5CH(OR)2 (R = alkyl, aryl). Bensylidenacetaler används som skyddsgrupper i glykemi. Dessa föreningar kan också oxideras till karboxylsyror för att öppna viktiga biologiska molekyler, t.ex. glykosaminoglykaner, för andra syntesvägar. De uppstår vid reaktion av en 1,2- eller 1,3-diol med bensaldehyd. Andra aromatiska aldehyder används också. (sv) |
| dbo:thumbnail | wiki-commons:Special:FilePath/Bngluc.png?width=300 |
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| dbo:wikiPageLength | 1937 (xsd:nonNegativeInteger) |
| dbo:wikiPageRevisionID | 1028200782 (xsd:integer) |
| dbo:wikiPageWikiLink | dbr:Protecting_group dbc:Acetals dbc:Protecting_groups dbr:Organic_chemistry dbr:Diol dbc:Functional_groups dbr:File:Bngluc.png |
| dct:subject | dbc:Acetals dbc:Protecting_groups dbc:Functional_groups |
| rdfs:comment | In organic chemistry, a benzylidene acetal is the functional group with the structural formula C6H5CH(OR)2 (R = alkyl, aryl). Benzylidene acetals are used as protecting groups in glycochemistry. These compounds can also be oxidized to carboxylic acids in order to open important biological molecules, such as glycosaminoglycans, to other routes of synthesis. They arise from the reaction of a 1,2- or 1,3-diols with benzaldehyde. Other aromatic aldehydes are also used. (en) Bensylidenacetal är inom organisk kemi en funktionell grupp med strukturformeln C6H5CH(OR)2 (R = alkyl, aryl). Bensylidenacetaler används som skyddsgrupper i glykemi. Dessa föreningar kan också oxideras till karboxylsyror för att öppna viktiga biologiska molekyler, t.ex. glykosaminoglykaner, för andra syntesvägar. De uppstår vid reaktion av en 1,2- eller 1,3-diol med bensaldehyd. Andra aromatiska aldehyder används också. (sv) |
| rdfs:label | Benzylidene acetal (en) Bensylidenacetal (sv) |
| owl:sameAs | wikidata:Benzylidene acetal dbpedia-fa:Benzylidene acetal dbpedia-sv:Benzylidene acetal http://ta.dbpedia.org/resource/பென்சிலிடின்_அசிட்டால் https://global.dbpedia.org/id/5Ji1B |
| prov:wasDerivedFrom | wikipedia-en:Benzylidene_acetal?oldid=1028200782&ns=0 |
| foaf:depiction | wiki-commons:Special:FilePath/Bngluc.png |
| foaf:isPrimaryTopicOf | wikipedia-en:Benzylidene_acetal |
| is dbo:wikiPageWikiLink of | dbr:Benzaldehyde dbr:Benzylidene_compounds dbr:Acetal |
| is foaf:primaryTopic of | wikipedia-en:Benzylidene_acetal |
