N,N-Diethyl-1-Tosyl-3-Indoleglyoxylamide as a Dienophile in Diels-Alder Reactions. Hyperbaric vs. Thermal Conditions

Biolatto, B.; Kneeteman, M.; Mancini, P. M.

doi:10.3390/50300393

Volume 5, Issue 3

Article Versions

Related Info

More by Authors

Export Article

Open AccessAbstract

Molecules 2000, 5(3), 393-395; https://doi.org/10.3390/50300393

N,N-Diethyl-1-Tosyl-3-Indoleglyoxylamide as a Dienophile in Diels-Alder Reactions. Hyperbaric vs. Thermal Conditions

B. Biolatto, M. Kneeteman and P. M. Mancini *

Laboratorio Fester, Dpto. de Química, Facultad de Ingeniería Química, Universidad Nacional del Litoral, Santiago del Estero 2829, 3000, Santa Fe, Argentina

Author to whom correspondence should be addressed.

Published: 22 March 2000

Full-Text | PDF [20 KB, uploaded 18 June 2014] |

Figures

Abstract

Under high pressure conditions, the Diels-Alder reaction involving N,N-diethyl-1-tosyl-3-indoleglyoxylamide and 1-(N-acetyl-N-propylamino)-1,3-butadiene produces a highly functionalized intermediate for the synthesis of Indole Alkaloids, in shorter times and higher yields than under thermal conditions. View Full-Text

▼ Figures

Scheme 1

This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

Share & Cite This Article

MDPI and ACS Style

Biolatto, B.; Kneeteman, M.; Mancini, P.M. N,N-Diethyl-1-Tosyl-3-Indoleglyoxylamide as a Dienophile in Diels-Alder Reactions. Hyperbaric vs. Thermal Conditions. Molecules 2000, 5, 393-395.