Click-chemistry approach to azacycloalkene monosulfonyl diamines: synthesis and computational analysis of the reaction mechanism

被引:27
作者
Contini, Alessandro [1 ]
Erba, Emanuela [1 ]
机构
[1] Univ Milan, Ctr Interuniv Ric Reaz Pericicl & Sintesi Sistemi, Dipartimento Sci Farmaceut, Sez Chim Gen & Organ Alessandro Marchesini, I-20133 Milan, Italy
关键词
ASYMMETRIC TRANSFER HYDROGENATION; MOLECULAR-ENERGIES; VIC-TRIAZOLINES; V-TRIAZOLINES; CYCLOADDITIONS; ACIDS;
D O I
10.1039/c2ra21592f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The cycloaddition reaction of the morpholino enamines of N-methylpiperidone and N-methyl tropinone with sulfonylazides was exploited, leading to a click-chemistry approach to uncommon azacycloalkene monosulfonyl diamines in good yields. A computational model for the key step decomposition of the triazoline intermediate was then realized by DFT calculations. The model explains the observed reaction outcome and leads to a new interpretation of the decomposition mechanism for 5-amino-1,2,3-triazolines.
引用
收藏
页码:10652 / 10660
页数:9
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