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首页> 外文期刊>Bulletin of the Chemical Society of Japan >Optically Active Seleninic Acid:Isolation,Absolute Configuration,Stability,and Chiral Crystallization
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Optically Active Seleninic Acid:Isolation,Absolute Configuration,Stability,and Chiral Crystallization

机译:旋光性硒酸:分离,绝对构型,稳定性和手性结晶

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摘要

Each optical isomer of methaneseleninic acid (la) was isolated as chiral crystals by recrystallization from meth-anol/toluene.The absolute configuration of one of the enantiomers was determined by X-ray crystallographic analysis,and the relationship between the absolute configuration and the circular dichroism spectra of la was clarified.The optically active seleninic acid (R)-la was stable toward racemization in the solid state,although it racemized very rapidly in solution.Each enantiomer of la was obtained in bulk by chiral crystallization in the presence of a seed crystal or chiral solvents.The absolute configuration of optically active methanesulfinic acid (4) was also assigned by comparing its circular dichroism spectra with those of la.
机译:通过从甲醇/甲苯中重结晶,分离出甲烷硒酸(la)的每种旋光异构体,形成手性晶体。通过X射线晶体学分析确定一种对映异构体的绝对构型,并确定其与环状结构的关系。澄清了la的二向色光谱。旋光性硒酸(la)-la在固态下对消旋稳定,尽管在溶液中消旋非常迅速。在a的存在下通过手性结晶大量获得了la的每个对映异构体还通过将其圆二色性光谱与la的圆二色性光谱进行比较,确定了光学活性甲亚磺酸(4)的绝对构型。

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