Reactions of 2, 3-diaryl-1-methyl-4, 5-dihydroimidazolium iodides with nucleophilic reagents
C Xia, J Hao, Y Tang, Y Ni, P Zhou
Index: Xia, Chizhong; Hao, Junsheng; Tang, Yiqing; Ni, Yanping; Zhou, Peiwen Synthetic Communications, 2002 , vol. 32, # 9 p. 1457 - 1464
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Citation Number: 4
Abstract
ABSTRACT 2, 3-Diaryl imidazolium salts, represented by 1 and 2, reacted with 2- ethanolamine or ethylenediamine to produce 2-aryl oxazolines or imidazolines 5–8 respectively. Their hydrolysis resulted in ring-opened ethylenediamine derivatives 9 and 10. The reduction of 1 and 2 produced partially reduced imidazolidines 11, 12 and 11 reacted further with tryptamine to provide 2, 3, 4, 9-tetrahydro-1-phenyl 1 H-pyrido [3, 4-b] indole, ...
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