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Esters, hydroxy Ritter reaction

Application of the Ritter reaction conditions on y-hydroxy-a,P-alkynoic esters, 102, produced ethyl 5-oxazoleacetates 103 or y-A-acylamino-P-keto ester 104 by reaction with aryl or alkyl nitriles respectively. The y-A-acylamino-P-keto ester 104 can also be transformed into oxazole derivatives using an additional step involving POCI3 <06TL4385>. [Pg.299]


See other pages where Esters, hydroxy Ritter reaction is mentioned: [Pg.115]    [Pg.146]    [Pg.146]    [Pg.139]    [Pg.135]    [Pg.127]    [Pg.311]   
See also in sourсe #XX -- [ Pg.6 , Pg.268 ]

See also in sourсe #XX -- [ Pg.6 , Pg.268 ]




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Hydroxy esters

Hydroxy reaction

Ritter

Ritter Reaction

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