化学
酰胺
双环分子
戒指(化学)
水解
药物化学
立体化学
有机化学
作者
C. Heidelberger,Armin Guggisberg,Euripides Stephanon,Manfred Hesse
标识
DOI:10.1002/hlca.19810640205
摘要
Amidines as Intermediates in Transamidation Reactions By loss of water in the presence of p ‐toluenesulfonic acid/xylole N ‐aminoalkyllactames form bicyclic amidines. The corresponding N ‐alkylaminoalkyl‐lactames' react to bicyclic amidinium salts or to transamidated products, ring‐enlarged by the N ‐alkylamino residue, respectively (s. Scheme 1 ). The bicyclic amidines and amidinium salts are partially hydrolyzed by KOH/H 2 O to lactames (s. Scheme 2 ). Which of the two possible isomeric lactames are formed is discussed.
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