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首页> 外文期刊>Organic letters >Asymmetric Synthesis of #alpha#-#beta#-Dialkyl-#alpha#-phenylalanines via Direct Alkylation of a Chiral Alanine Derivative with Racemic #alpha#-Alkylbenzyl Bromides.A Case of High Enantiomer Differentiation of Room Temperature
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Asymmetric Synthesis of #alpha#-#beta#-Dialkyl-#alpha#-phenylalanines via Direct Alkylation of a Chiral Alanine Derivative with Racemic #alpha#-Alkylbenzyl Bromides.A Case of High Enantiomer Differentiation of Room Temperature

机译:通过手性丙氨酸衍生物与外消旋的#α#-烷基苄基溴的直接烷基化反应不对称合成#α#-β-二烷基-αα-苯丙氨酸。室温下高对映异构体差异的情况

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摘要

This study demonstrates that the direct alkylation of a Ni(II)-complex of the chirla Schiff base of alanine with (S)-o-[N-(N-bnezylprolyl)amino]-benzophenone,with racemic #alpha#-alkylbenzyl bromides,is a synthetically feasible and methodologically advantageous approach to the target #alpha#,#beta#-dialkylphenylalanines over previously reported methods.For the first time we report and rationalize a case of a high enantiomer differentiation process at room temperature.
机译:这项研究表明丙氨酸的希夫席夫希夫碱的Ni(II)配合物与(S)-o- [N-(N-(n-(ne-bnezylprolyl)amino]-苯甲酮)与外消旋#alpha#-烷基苄基溴的直接烷基化相对于先前报道的方法,是对目标α-α,β-二烷基苯丙氨酸的合成可行和方法学上有利的方法。首次我们报道并合理化了室温下高对映异构体分化过程的情况。

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