首页> 外文期刊>Russian Journal of Organic Chemistry >Synthesis and aminolysis of N-(bicyclo[2.2.1]hept-5-en-endo-2-ylmethyl)-N-(oxiran-2-ylmethyl)(7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonamide
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Synthesis and aminolysis of N-(bicyclo[2.2.1]hept-5-en-endo-2-ylmethyl)-N-(oxiran-2-ylmethyl)(7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonamide

机译:N-(双环[2.2.1]庚-5-烯-内-2-基甲基)-N-(环氧乙烷-2-基甲基)(7,7-二甲基-2-氧双环[2.2.1]的合成​​和氨解庚基-1-基)甲磺酰胺

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摘要

A new N-(oxiran-2-ylmethyl) (glycidyl) derivative has been obtained by reaction of N-(bicyclo-[2.2.1]hept-5-en-endo-2-ylmethyl)(7,7-dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonamide with epichlorohydrin. Its epoxidation and aminolysis have been studied, and the regioselectivity of these transformations has been determined by IR and H-1 NMR spectroscopy and mass spectrometry.
机译:通过N-(双环[[2.2.1]庚-5-烯-内-2-基甲基)(7,7-二甲基-)的反应获得了新的N-(环氧乙烷-2-基甲基)(缩水甘油基)衍生物。 2-环氧双环[2.2.1]庚-1-基)甲磺酰胺与表氯醇。已经研究了其环氧化和氨解,并通过IR和H-1 NMR光谱和质谱确定了这些转化的区域选择性。

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