Aminomercuration intramoleculaire d'aziridines cycloocteniques et de leurs aminoalcools precurseurs
作者:M. Barrelle、M. Apparu
DOI:10.1016/0040-4020(77)84078-7
日期:1977.1
cyclooctenic aziridines undergo intramolecular mercuration with mercuric salts; after reduction, N-substituted 9-azabicyclo[3.3.1]- and [4.2.1]nonanes are isolated. Mercuration of amino alcohols (precursors to aziridines) leads to the same products but with different yields dependent on the mercuric salt used. In some cases, aziridinium salts are intermediates in basic medium from the organo mercuric compounds
N-取代的环辛烯二氮丙啶与汞盐一起进行分子内汞化;还原后,分离出N-取代的9-氮杂双环[3.3.1]-和[4.2.1]壬烷。氨基醇(前体为氮丙啶)的汞化可得到相同的产品,但取决于所用的汞盐,其收率不同。在某些情况下,叠氮鎓盐是碱性介质中还原过程中来自有机汞化合物的中间体。用两种脂族模型研究了该反应的扩展。