首页> 外文期刊>Synthetic Communications >AN IMPROVED REDUCTION PROCEDURE IN THE SYNTHESIS OF SUBSTITUTED PYRROLIDINES VIA AN AMINOMERCURATION REDUCTION SEQUENCE OF PRIMARY ALKENYLAMINES
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AN IMPROVED REDUCTION PROCEDURE IN THE SYNTHESIS OF SUBSTITUTED PYRROLIDINES VIA AN AMINOMERCURATION REDUCTION SEQUENCE OF PRIMARY ALKENYLAMINES

机译:通过原链烯酰胺的胺化还原序列合成取代的吡咯烷酮的改进还原方法

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摘要

Aminomercuration/reduction sequence of delta-alkenylamines is a typical route to substituted pyrrolidines. Backward reaction to the starting material is a major drawback which occurs during sodium borohydride reduction of the intermediate organomercurial. We describe here a new reduction procedure which prevents almost completely this backward reaction and leads to significant increases in the yields of pyrrolidines. [References: 44]
机译:δ-烯基胺的胺基化/还原序列是取代吡咯烷的典型途径。与起始原料的向后反应是主要的缺点,其在中间有机汞的硼氢化钠还原过程中发生。我们在这里描述了一种新的还原程序,该程序几乎完全防止了这种逆反应,并导致吡咯烷的收率显着提高。 [参考:44]

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