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Oxazolidinone, carboxylic acid, double

A similar approach towards norbornane carboxylic acid derivatives was developed using pseudoenantiomeric A-acyl-D-galactosyl and D-arabinosyl-oxazolidinones 96 and 97. Reaction with cyclopentadiene under promotion of Me2AlCl, and subsequent hydrogenolysis of the double bond and basic hydrolysis of the imide moiety, furnished the 3-methyl-norbornane-2-carboxylic acids 98 and 99, respectively, in high enantiomeric purity [74,75] (Scheme 10.32). [Pg.457]

A Double Decarboxylation Reaction of an Oxazolidinone and a Carboxylic Acid ... [Pg.187]

A Double Decarboxylation Reaction of an Oxazolidinone and a Carboxylic Acid Its Application to the Synthesis of a New Opioid Lead Compound [45]... [Pg.203]

See other pages where Oxazolidinone, carboxylic acid, double is mentioned: [Pg.29]    [Pg.571]    [Pg.187]    [Pg.22]    [Pg.22]   


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