Synthesis and resolution of DL-phenylalanine analogues
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    Abstract:

    Objective:Synthesis of L-2,6-dimethylphenylalanine and L-2,4,6-trimethylphenylalanine through enzymatic resolution. Methods:Racemic 2,6-dimethylphenylalanine and 2,4,6-trimethylphenylalanine were synthesized through reaction of diethyl acetamidomalonate with 2,6-dimethylbenzyl bromide or 2,4,6-trimethylbenzyl bromide,respectively. The DL-amino acids were then enzymatically resoluted by L-amino acylase. Results:Racemic 2,6-dimethylphenylalanine and 2,4,6-trimethylphenylalanine were synthesized through reaction of diethyl acetamidomalonate with 2,6-dimethylbenzyl bromide and 2,4,6-trimethylbenzyl bromide in yield of 87.9% and 86.0% respectively;DL-2,6-dimethylphenylalanine was successfully resoluted by L-amino acylase,but it was failed in the resolution of 2,4,6-trimethylphenylalanine. Conclusion:L-amino acylase can be used in the resolution of DL-2,6-dimethylphenylalanine,but it is ineffective in the resolution of 2,4,6-trimethylphenylalanine.

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刘金春,宋博文,马 玉,蔡 俊,厉廷有. DL-苯丙氨酸类似物的合成及其拆分[J].南京医科大学学报(自然科学版英文版),2013,(3):412-415.

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History
  • Received:November 23,2012
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  • Online: June 04,2013
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