Diastereoselective Synthesis of Dihydroisoindolo[2,1‑a]quinolin-11- ones by Solvent-Free AMCell-SO3H‑Catalyzed Imino Diels−Alder/Intramolecular Amide Cyclization Cascade Reactions

Nineteen bioactive highly functionalized 6,6a-dihydroisoindolo[2,1-a]quinolin-11(5H)-one derivatives were easily prepared in good yield without solvent using catalytic amorphous milled cellulose sulfonic acid (AMCell-SO3H), substituted anilines, propenyl-phenols, and phthaldehydic acid. The cascade reaction gave high regioselectivity and diastereoselectivity.

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Main Authors: Merchan Arenas, Diego Rolando, Kouznetsov, Vladimir V.
Format: Artículo científico biblioteca
Language:eng
Published: 2014-04-30
Subjects:Biología vegetal, Aceites vegetales, Productos químicos, Biología molecular, Biotecnología, Aceites esenciales, Tecnología química, Química agrícola,
Online Access:http://repositorio.colciencias.gov.co/handle/11146/34169
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spelling dig-minciencias-co-20.500.14143-341692023-11-29T12:38:17Z Diastereoselective Synthesis of Dihydroisoindolo[2,1‑a]quinolin-11- ones by Solvent-Free AMCell-SO3H‑Catalyzed Imino Diels−Alder/Intramolecular Amide Cyclization Cascade Reactions Merchan Arenas, Diego Rolando Kouznetsov, Vladimir V. Biología vegetal Aceites vegetales Productos químicos Biología molecular Biotecnología Aceites esenciales Tecnología química Química agrícola Nineteen bioactive highly functionalized 6,6a-dihydroisoindolo[2,1-a]quinolin-11(5H)-one derivatives were easily prepared in good yield without solvent using catalytic amorphous milled cellulose sulfonic acid (AMCell-SO3H), substituted anilines, propenyl-phenols, and phthaldehydic acid. The cascade reaction gave high regioselectivity and diastereoselectivity. Departamento Administrativo de Ciencia, Tecnología e Innovación [CO] Colciencias 5507-543-31904 Programa: Bioprospección y desarrollo de ingredientes naturales para las industrias cosmética, farmacéutica y de productos de aseo con base en la biodiversidad colombiana no 2019-04-01T00:03:12Z 2019-04-01T00:03:12Z 2014-04-30 info:eu-repo/date/embargoEnd/2024-01-31 Artículo científico info:eu-repo/semantics/publishedVersion info:eu-repo/semantics/article http://repositorio.colciencias.gov.co/handle/11146/34169 Contiene 37 referencias bibliográficas. Véase documento adjunto 10.1021/jo500516c eng Programa: Bioprospección y desarrollo de ingredientes naturales para las industrias cosmética, farmacéutica y de productos de aseo con base en la biodiversidad colombiana. La publicación completa está disponible en : <a href="http://repositorio.colciencias.gov.co/handle/11146/34163" target="blank">http://repositorio.colciencias.gov.co/handle/11146/34163</a> info:eu-repo/semantics/embargoedAccess pdf 7 páginas application/pdf Colombia The Journal of Organic Chemistry 2014, 79, 5327−5333
institution MINCIENCIAS CO
collection DSpace
country Colombia
countrycode CO
component Bibliográfico
access En linea
databasecode dig-minciencias-co
tag biblioteca
region America del Sur
libraryname Centro de Documentación y Biblioteca de MINCIENCIAS de Colombia
language eng
topic Biología vegetal
Aceites vegetales
Productos químicos
Biología molecular
Biotecnología
Aceites esenciales
Tecnología química
Química agrícola
Biología vegetal
Aceites vegetales
Productos químicos
Biología molecular
Biotecnología
Aceites esenciales
Tecnología química
Química agrícola
spellingShingle Biología vegetal
Aceites vegetales
Productos químicos
Biología molecular
Biotecnología
Aceites esenciales
Tecnología química
Química agrícola
Biología vegetal
Aceites vegetales
Productos químicos
Biología molecular
Biotecnología
Aceites esenciales
Tecnología química
Química agrícola
Merchan Arenas, Diego Rolando
Kouznetsov, Vladimir V.
Diastereoselective Synthesis of Dihydroisoindolo[2,1‑a]quinolin-11- ones by Solvent-Free AMCell-SO3H‑Catalyzed Imino Diels−Alder/Intramolecular Amide Cyclization Cascade Reactions
description Nineteen bioactive highly functionalized 6,6a-dihydroisoindolo[2,1-a]quinolin-11(5H)-one derivatives were easily prepared in good yield without solvent using catalytic amorphous milled cellulose sulfonic acid (AMCell-SO3H), substituted anilines, propenyl-phenols, and phthaldehydic acid. The cascade reaction gave high regioselectivity and diastereoselectivity.
format Artículo científico
topic_facet Biología vegetal
Aceites vegetales
Productos químicos
Biología molecular
Biotecnología
Aceites esenciales
Tecnología química
Química agrícola
author Merchan Arenas, Diego Rolando
Kouznetsov, Vladimir V.
author_facet Merchan Arenas, Diego Rolando
Kouznetsov, Vladimir V.
author_sort Merchan Arenas, Diego Rolando
title Diastereoselective Synthesis of Dihydroisoindolo[2,1‑a]quinolin-11- ones by Solvent-Free AMCell-SO3H‑Catalyzed Imino Diels−Alder/Intramolecular Amide Cyclization Cascade Reactions
title_short Diastereoselective Synthesis of Dihydroisoindolo[2,1‑a]quinolin-11- ones by Solvent-Free AMCell-SO3H‑Catalyzed Imino Diels−Alder/Intramolecular Amide Cyclization Cascade Reactions
title_full Diastereoselective Synthesis of Dihydroisoindolo[2,1‑a]quinolin-11- ones by Solvent-Free AMCell-SO3H‑Catalyzed Imino Diels−Alder/Intramolecular Amide Cyclization Cascade Reactions
title_fullStr Diastereoselective Synthesis of Dihydroisoindolo[2,1‑a]quinolin-11- ones by Solvent-Free AMCell-SO3H‑Catalyzed Imino Diels−Alder/Intramolecular Amide Cyclization Cascade Reactions
title_full_unstemmed Diastereoselective Synthesis of Dihydroisoindolo[2,1‑a]quinolin-11- ones by Solvent-Free AMCell-SO3H‑Catalyzed Imino Diels−Alder/Intramolecular Amide Cyclization Cascade Reactions
title_sort diastereoselective synthesis of dihydroisoindolo[2,1‑a]quinolin-11- ones by solvent-free amcell-so3h‑catalyzed imino diels−alder/intramolecular amide cyclization cascade reactions
publishDate 2014-04-30
url http://repositorio.colciencias.gov.co/handle/11146/34169
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AT kouznetsovvladimirv diastereoselectivesynthesisofdihydroisoindolo21aquinolin11onesbysolventfreeamcellso3hcatalyzediminodielsalderintramolecularamidecyclizationcascadereactions
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