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通过醌基 α,α-氨基酸酯的氧化脱羧反应,前所未有地合成了一种新型的氨基醌环系统。

Unprecedented synthesis of a novel amino quinone ring system via oxidative decarboxylation of quinone-based alpha,alpha-amino esters.

机构信息

Department of Pharmaceutical Science, University of Salerno, I-84084, Fisciano, Salerno, Italy.

出版信息

Org Biomol Chem. 2010 Feb 7;8(3):622-7. doi: 10.1039/b918898c. Epub 2009 Dec 8.

DOI:10.1039/b918898c
PMID:20090979
Abstract

An unusual and efficient method for the synthesis of new quinone-based amine and its derivatives from the corresponding alpha,alpha-amino ester is described. The procedure involves the quinone-based system's oxidative decarboxylation via hydride transfer throughout basic hydrolysis. This synthetic method provides, with good yields, rapid access to new potentially cytotoxic quinones.

摘要

描述了一种从相应的α,α-氨基酸酯合成新型醌基胺及其衍生物的独特而有效的方法。该方法涉及通过氢化物转移在碱性水解过程中醌基体系的氧化脱羧。这种合成方法以良好的收率提供了快速获得新型潜在细胞毒性醌的途径。

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