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新型生物活性杂环化合物的合成与抗菌活性:10h - 吩噻嗪及其核糖呋喃糖苷和砜衍生物

Synthesis and antimicrobial activities of novel biologically active heterocycles: 10h-phenothiazines, their ribofuranosides, and sulfone derivatives.

作者信息

Dixit Yogesh, Dixit Rahul, Gautam Naveen, Gautam D C

机构信息

Department of Chemistry, University of Rajasthan, Jaipur, India.

出版信息

Nucleosides Nucleotides Nucleic Acids. 2009 Nov;28(11):998-1006. doi: 10.1080/15257770903362206.

Abstract

This article deals with the synthesis and antimicrobial activity of a series of novel substituted 10H-phenothiazines, their ribofuranosides, and sulfone derivatives. 10H-Phenothiazines were prepared by Smiles rearrangement. These prepared phenothiazines were used as the base to prepare ribofuranosides by treatment with sugar (1-O-acetyl-2,3,5-tri-O-benzoylribofuranose). Sulfone derivatives were prepared by the oxidation of 10H-phenothiazines. The structure of the synthesized compounds was established by elemental analysis and spectroscopic data.

摘要

本文研究了一系列新型取代的10H-吩噻嗪及其核糖呋喃糖苷和砜衍生物的合成与抗菌活性。通过斯迈尔斯重排反应制备了10H-吩噻嗪。这些制备好的吩噻嗪作为基础原料,通过与糖(1-O-乙酰基-2,3,5-三-O-苯甲酰基核糖呋喃糖)反应来制备核糖呋喃糖苷。砜衍生物则通过10H-吩噻嗪的氧化反应制备。通过元素分析和光谱数据确定了合成化合物的结构。

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