Syntheses of armed??macrocycles by reductive amination using NaBH (OAc) 3 under 1 MPa

Y Habata, F Osaka, S Yamada

Index: Habata, Yoichi; Osaka, Futoshi; Yamada, Sachiko Journal of Heterocyclic Chemistry, 2006 , vol. 43, # 1 p. 157 - 161

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Citation Number: 7

Abstract

Armed-monoaza-12-crown-4, monoaza-15-crown-5, diaza-12-crown-4, diaza-18-crown-6 ethers, and 1, 4, 7, 10-tetraazacyclododecane having aromatic pendants were prepared by the reductive amination of the corresponding macrocycles with aromatic carboxyaldehydes in the presence of NaBH (OAc) 3. Reductive amination under 1 MPa conditions provided significant shortening of the reaction time and yield enhancements.