One-pot synthesis of acenaphtho[1,2-b]pyrroles in the presence of supported ionic liquid catalyst

被引：1
|
作者：
Sandaroos, Reza [1 ,2 ]
Goldani, Mohammad Taghi [1 ,2 ]
Damavandi, Saman [3 ]
机构：
[1] Univ Birjand, Dept Chem, Fac Sci, Birjand, Iran
[2] Islamic Azad Univ, Dept Chem, Birjand Branch, Birjand, Iran
[3] Islamic Azad Univ, Dept Chem, Sarvestan Branch, Sarvestan, Iran
来源：
HETEROCYCLIC COMMUNICATIONS | 2012年 / 18卷 / 03期
关键词：
acenaphtho[1,2-b]pyrrole-8-amine; isocyanides; one-pot reaction; BAEYER-VILLIGER-OXIDATION; PROTOCOL; ETHERS;
D O I：
10.1515/hc-2011-0126
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Eleven new 8-[(alkyl or aryl)amino]-9-(alkyl or aryl)acenaphtho[1,2-b]pyrroles were synthesized by one-pot reaction of (acenaphthylen-1-yloxy)trimethylsilane, alkyl or aryl aldehyde, ammonium acetate, and aryl or alkyl isocyanide in refluxing DMF.
引用
收藏
页码：157 / 160
页数：4
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