氨基吡啶
化学
氘
喹啉
微波辐射
同位素
催化作用
微波食品加热
辐照
有机化学
分子
量子力学
物理
核物理学
作者
Mark C. Bagley,Ayed Alnomsy,Hussein Inayah Sharhan
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2016-08-03
卷期号:27 (17): 2467-2472
被引量:8
标识
DOI:10.1055/s-0035-1562479
摘要
4-Aminopyridines undergo surprisingly rapid and highly-selective H/D exchange at C-2 and C-6 in neutral D2O upon microwave irradiation at only 190 °C for 2 h in a sealed vessel. This method contrasts and complements acid-mediated H/D exchange, requires no catalyst and is appropriate for the synthesis of deuterium isotop-ologues of N- and C-substituted 4-aminopyridines and a ben-zofused (quinoline) analogue.
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