Aminoalkylbenzotriazoles: reagents for the aminoalkylation of electron rich heterocycles
作者:Alan R. Katritzky、Zhijun Yang、Jamshed N. Lam
DOI:10.1016/s0040-4020(01)81590-8
日期:1992.6
Secondary and tertiary aminoalkylbenzotriazoles react with pyrrole, indole, their N-methyl analogs and with 2-methylfuran under mild reaction conditions in the presence of a Lewis acid to afford selectively the corresponding secondary or tertiary amines.
Solvent-Free Aminoalkylation of Phenols and Indoles Assisted by Microwave Irradiation
Phenols and indoles were aminoalkylated in a solvent-free and environmentally friendly Mannich reaction on acidic alumina assisted by microwave irradiation in good overall yields.
MORIYA TAMON; MORIYA TAMON; HAGIO KATSUAKI; HAGIO KATSUAKI; YONEDA NAOTO;+, CHEM. AND PHARM. BULL., 1980, 28, NO 6, 1711-1721