Catalytic Addition of Indole-2-Carboxylic Acid to 1-Hexyne

The synthesis of two novel enol esters, namely hex-1-en-2-yl indole-2-carboxylate and hex-1-en-2-yl 1-(hex-1-en-2-yl)-indole-2-carboxylate, is presented. Both compounds were generated by addition of indole-2-carboxylic acid to 1-hexyne employing [RuCl<sub>2</sub>(<i>η</i><...

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Main Authors: Javier Francos, Alba E. Díaz-Álvarez, Victorio Cadierno
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Molbank
Subjects:
Online Access:https://www.mdpi.com/1422-8599/2020/3/M1145
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author Javier Francos
Alba E. Díaz-Álvarez
Victorio Cadierno
author_facet Javier Francos
Alba E. Díaz-Álvarez
Victorio Cadierno
author_sort Javier Francos
collection DOAJ
description The synthesis of two novel enol esters, namely hex-1-en-2-yl indole-2-carboxylate and hex-1-en-2-yl 1-(hex-1-en-2-yl)-indole-2-carboxylate, is presented. Both compounds were generated by addition of indole-2-carboxylic acid to 1-hexyne employing [RuCl<sub>2</sub>(<i>η</i><sup>6</sup>-<i>p</i>-cymene)(PPh<sub>3</sub>)] and [AuCl(PPh<sub>3</sub>)]/AgPF<sub>6</sub>, respectively, as catalysts.
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spelling doaj.art-31984c3d8efb4c9ab192742ac02a073d2023-11-20T05:49:19ZengMDPI AGMolbank1422-85992020-07-0120203M114510.3390/M1145Catalytic Addition of Indole-2-Carboxylic Acid to 1-HexyneJavier Francos0Alba E. Díaz-Álvarez1Victorio Cadierno2Laboratorio de Compuestos Organometálicos y Catálisis (Unidad Asociada al CSIC), Departamento de Química Orgánica e Inorgánica, Facultad de Química, Universidad de Oviedo, Julián Clavería 8, E-33006 Oviedo, SpainLaboratorio de Compuestos Organometálicos y Catálisis (Unidad Asociada al CSIC), Departamento de Química Orgánica e Inorgánica, Facultad de Química, Universidad de Oviedo, Julián Clavería 8, E-33006 Oviedo, SpainLaboratorio de Compuestos Organometálicos y Catálisis (Unidad Asociada al CSIC), Departamento de Química Orgánica e Inorgánica, Facultad de Química, Universidad de Oviedo, Julián Clavería 8, E-33006 Oviedo, SpainThe synthesis of two novel enol esters, namely hex-1-en-2-yl indole-2-carboxylate and hex-1-en-2-yl 1-(hex-1-en-2-yl)-indole-2-carboxylate, is presented. Both compounds were generated by addition of indole-2-carboxylic acid to 1-hexyne employing [RuCl<sub>2</sub>(<i>η</i><sup>6</sup>-<i>p</i>-cymene)(PPh<sub>3</sub>)] and [AuCl(PPh<sub>3</sub>)]/AgPF<sub>6</sub>, respectively, as catalysts.https://www.mdpi.com/1422-8599/2020/3/M1145enol estershydro-oxycarbonylation reactionshydroamination reactionsruthenium catalystsgold catalysts
spellingShingle Javier Francos
Alba E. Díaz-Álvarez
Victorio Cadierno
Catalytic Addition of Indole-2-Carboxylic Acid to 1-Hexyne
Molbank
enol esters
hydro-oxycarbonylation reactions
hydroamination reactions
ruthenium catalysts
gold catalysts
title Catalytic Addition of Indole-2-Carboxylic Acid to 1-Hexyne
title_full Catalytic Addition of Indole-2-Carboxylic Acid to 1-Hexyne
title_fullStr Catalytic Addition of Indole-2-Carboxylic Acid to 1-Hexyne
title_full_unstemmed Catalytic Addition of Indole-2-Carboxylic Acid to 1-Hexyne
title_short Catalytic Addition of Indole-2-Carboxylic Acid to 1-Hexyne
title_sort catalytic addition of indole 2 carboxylic acid to 1 hexyne
topic enol esters
hydro-oxycarbonylation reactions
hydroamination reactions
ruthenium catalysts
gold catalysts
url https://www.mdpi.com/1422-8599/2020/3/M1145
work_keys_str_mv AT javierfrancos catalyticadditionofindole2carboxylicacidto1hexyne
AT albaediazalvarez catalyticadditionofindole2carboxylicacidto1hexyne
AT victoriocadierno catalyticadditionofindole2carboxylicacidto1hexyne