Issue 23, 1993

Novel efficient synthesis of 1-ethoxyvinyl esters using ruthenium catalysts and their use in acylation of amines and alcohols: synthesis of hydrophilic 3′-N-acylated oxaunomycin derivatives

Abstract

A novel and efficient synthesis of 1-ethoxyvinyl esters 3ai from carboxylic acids 4ai and ethoxyacetylene 5 by using a catalytic amount of ruthenium complex [{RuCl2(p-cymene)}2]6f has been developed. These reagents reacted smoothly with amines and alcohols to give the corresponding N- and O-acylated compounds in excellent yields. This acylation method has been applied to the synthesis of hydrophilic 3′-N-acylated oxaunomycin derivatives 13a, b.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1993, 2999-3005

Novel efficient synthesis of 1-ethoxyvinyl esters using ruthenium catalysts and their use in acylation of amines and alcohols: synthesis of hydrophilic 3′-N-acylated oxaunomycin derivatives

Y. Kita, H. Maeda, K. Omori, T. Okuno and Y. Tamura, J. Chem. Soc., Perkin Trans. 1, 1993, 2999 DOI: 10.1039/P19930002999

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