Chemischer Informationsdienst. Organische Chemie
 1971
DOI: 10.1002/chin.197114432
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ChemInform Abstract: EINE VERBESSERTE SYNTH. VON L‐HISTIDIN‐BENZYLESTER

Arthur Félix1,
D. P. Winter2

Abstract: Bei Raumtemperatur reagiert N‐tert.‐Butoxycarbonyl‐L‐histidin (I) in Methanol mit einer ätherischen Lösung von Phenyldiazomethan zum Benzylester (II) (98% Ausbeute), der mit Salzsäure in Dioxan zum L‐Histidin‐benzylesterdihydrochlorid (III) hydrolysiert wird.

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