Acylation of nitrogen heterocycles. II . Carbobenzoxylation of substituted adenines under the conditions of the schotten‐baumann reaction

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<jats:title>Abstract</jats:title><jats:p>9‐Benzyladenine, 6‐benzylamino‐9‐benzyladenine, 6‐piperidino‐9‐benzyladenine and 2′,3′‐<jats:italic>O</jats:italic>‐isopropylidene‐5′‐trityladenosine underwent a Bamberger fission of the imidazole ring when treated with carbobenzoxy chloride in aqueous base. Under similar experimental conditions adenine itself afforded two monoacyl derivatives.</jats:p>

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