首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Direct synthesis of novel 2-imino-l,3-selenazolidine derivatives from OMICRON-methanesulfonyl beta-amino alcohol hydrochlorides
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Direct synthesis of novel 2-imino-l,3-selenazolidine derivatives from OMICRON-methanesulfonyl beta-amino alcohol hydrochlorides

机译:从OMICRON-甲磺酰基β-氨基醇盐酸盐直接合成新型2-亚氨基-1,3-硒代唑烷衍生物

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摘要

Recently,we have reported that 4,5-dialkylsubstituted 2-imino-l,3-azolidine derivatives(1)strongly inhibit inducible nitric oxide synthase(iNOS).To our knowledge,only few methods have been reported for the synthesis of 4,5-dialkylsubstituted 2-imino-l,3-selenazolidine derivatives(2),which are the selenium analogue of 1.Herein,we report the direct synthesis of 2 from the corresponding OMICRON-methanesulfonyl beta-amino alcohol hydrochlorides using potassium selenocyanate and evaluation for the inhibitory activity against iNOS of the newly synthesized selenazolidine derivatives.
机译:最近,我们报道了4,5-二烷基取代的2-亚氨基-1,3-氮杂环丁烷衍生物(1)强烈抑制诱导型一氧化氮合酶(iNOS)。据我们所知,只有很少的方法报道了4的合成方法。 5-二烷基取代的2-亚氨基-1,3-硒代唑烷衍生物(2),是1的硒类似物。在此,我们报道了使用硒氰酸钾从相应的OMICRON-甲磺酰基β-氨基醇盐酸盐直接合成2并进行评价合成的硒代硒唑烷衍生物对iNOS的抑制活性。

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