Health & Environmental Research Online (HERO)


Print Feedback Export to File
7597322 
Journal Article 
N-amination of pyrrole and indole heterocycles with monochloramine (NH2Cl) 
Hynes, J; Doubleday, WW; Dyckman, AJ; Godfrey, JD; Grosso, JA; Kiau, S; Leftheris, K 
2004 
Yes 
Journal of Organic Chemistry
ISSN: 0022-3263
EISSN: 1520-6904 
69 
1368-1371 
A survey of several electrophilic ammonia reagents for the N-amination of indole- and pyrrole-containing heterocycles revealed that monochloramine (NH2Cl) is an excellent reagent for this transformation. Pyrroles and indoles containing a variety of substitution were aminated on nitrogen with isolated yields ranging from 45% to 97%.