Next Article in Journal
Synthesis of Poly(m-pyridylene-1,2-diphenylvinylene)
Previous Article in Journal
Addition of Organotin Anions to α,β-Unsaturated Nitriles
Open AccessAbstract

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

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.
Molecules 2000, 5(3), 393-395; https://doi.org/10.3390/50300393
Published: 22 March 2000
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
Show Figures

Scheme 1

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. https://doi.org/10.3390/50300393

AMA Style

Biolatto B, Kneeteman M, Mancini PM. N,N-Diethyl-1-Tosyl-3-Indoleglyoxylamide as a Dienophile in Diels-Alder Reactions. Hyperbaric vs. Thermal Conditions. Molecules. 2000; 5(3):393-395. https://doi.org/10.3390/50300393

Chicago/Turabian Style

Biolatto, B.; Kneeteman, M.; Mancini, P. M. 2000. "N,N-Diethyl-1-Tosyl-3-Indoleglyoxylamide as a Dienophile in Diels-Alder Reactions. Hyperbaric vs. Thermal Conditions" Molecules 5, no. 3: 393-395. https://doi.org/10.3390/50300393

Find Other Styles

Article Access Map by Country/Region

1
Only visits after 24 November 2015 are recorded.
Search more from Scilit
 
Search
Back to TopTop