Reaction of N-(2,3-epoxypropyl)arenesulfonamides with (bicyclo[2.2.1]hept-5-en-endo-2-yl)methanamine

被引：0
|
作者：
L. I. Kas’yan
S. A. Prid’ma
A. V. Turov
V. A. Pal’chikov
A. O. Kas’yan
L. D. Karat
机构：
[1] Dnepropetrovsk National University,
[2] Taras Shevchenko Kiev National University,undefined
[3] ProBioGen A.G.,undefined
[4] Ukrainian Research Institutes of Plastics,undefined
来源：
Russian Journal of Organic Chemistry | 2009年 / 45卷
关键词：
Hydroxypropyl; Benzenesulfonamide; Amino Alcohol; Oxirane Ring; Methanamine;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
Reactions of bicyclo[2.2.1]hept-5-en-endo-2-ylmethanamine with N-(2,3-epoxypropyl)arenesulfonamides gave amino alcohols having a norbornene fragment and sulfonamide group. The major products were formed via opening of the oxirane ring according to the Krasuskii rule. The product structure was determined by 1H and 13C NMR spectroscopy using DEPT and two-dimensional COSY, NOESY, HMQC, and HMBC techniques.
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页码：505 / 511
页数：6
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