@misc{10481/82954,
year = {1986},
month = {3},
url = {https://hdl.handle.net/10481/82954},
abstract = {Se prepara 3-alquil-4-amino-2-metil-4,5,6,7-tetrahidroindol (lll) por reducción de 3-alquil-4-hidroxiimino-2-metil-4,5,6,7-tetrahidroindol (H) con Zn/AcOH. El compuesto II se ha obtenido por condensación de 3-alquil-2-metil-4-oxo-4,5,6,7-tetrahidroindol (I) con hidroxilamina. La reacción del compuesto (lll) con N-(2-cloroetil)-N,N-dimetilamina dá 3-alquil-4-[(2-dimetilarninoetil)arnino]-2-metil-4,5,6,7-tetrahidroindol (IV).},
abstract = {3-AIkyl-4-amino-2-methyl-4, 5, 6, 7-tetrahydroindole (lll) is synthetized by 
reduction of 3-aIkyl-4-hydroxyimino-2-methvl-4, 5, 6, 7-tetrahydroindole (Il) 
with Zn/HOAc. The compound 1I has been obtained by condensation of 3-aIkyl 2-methyl-4-oxo-4, 5, 6, 7-tetrahydroindole (1) with hydroxylarnine. The compound III give 3-alkyl-4-[(2-dimethylaminoethyl) arnino]-2 methyl-4, 5, 6, 7-tetrahydroindole (IV) by reaction with N-(2-chloroethyl)-N,N-dimethyla},
publisher = {Universidad de Granada, Facultad de Farmacia.},
title = {Síntesis de derivados de 4,5,5,7-tetrahidroindol},
author = {Domínguez Seglar, J. F. and Herrador Del Pino, María Del Mar and Sáenz de Buruaga Lerena, j},
}