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N-取代-α-氨基膦酸酯的不对称合成
The Asymmetric Synthesis of Chiral N - substituted - α-aminophosphonates
【摘要】 本文以手性α-异丙基对氯苄胺为手性诱导试剂和取代苯甲醛生成的席夫碱与亚磷酸酯进行不对称加成反应,生成具有双手性中心的N-取代-α-氨基膦酸酯。化学产率为40~91%,de%可达到72%。并简单讨论了立体效应对光学诱导能力的影响。
【Abstract】 Chiral N - substituted - α - aminophosphonates were synthesized stereoselectively by addition of dialkylphosphites and chiral imines, using ( S ) - α - iso - propylbenzylamine as chiral inducing agent. The de was up to 72 % and yields were 30 - 90 % . The stereoeffects on the optical and chemical yields were discussed briefly.
【关键词】 不对称合成;
手性席夫碱;
光学活性氯基膦酸酯;
【Key words】 asymmetric synthesis; chiral imine; N - substituted - α - aminophosphonate;
【Key words】 asymmetric synthesis; chiral imine; N - substituted - α - aminophosphonate;
- 【文献出处】 有机化学 ,Chinese Journal of Organic Chemistry , 编辑部邮箱 ,1996年03期
- 【分类号】O627.51
- 【被引频次】5
- 【下载频次】118