Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives

A small library of 3-hydroxyisoindolin-1-ones has been prepared from 3-alkylidenephtalides under ultrasonic irradiation. This practical synthesis is featured by group tolerance, high efficiency and yields. The reaction can also be performed in multigram scale and be further extended to access other...

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Autores principales: Mardjan, Muhammad Idham Darussalam, Hariadi, Muhamad Fadhly, Putri, Indah Mutiara, Musyarrofah, Nilna Amalia, Salimah, Muflihah, Priatmoko, Purwono, Bambang, Commeiras, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241359/
https://www.ncbi.nlm.nih.gov/pubmed/35873335
http://dx.doi.org/10.1039/d2ra02720h
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author Mardjan, Muhammad Idham Darussalam
Hariadi, Muhamad Fadhly
Putri, Indah Mutiara
Musyarrofah, Nilna Amalia
Salimah, Muflihah
Priatmoko,
Purwono, Bambang
Commeiras, Laurent
author_facet Mardjan, Muhammad Idham Darussalam
Hariadi, Muhamad Fadhly
Putri, Indah Mutiara
Musyarrofah, Nilna Amalia
Salimah, Muflihah
Priatmoko,
Purwono, Bambang
Commeiras, Laurent
author_sort Mardjan, Muhammad Idham Darussalam
collection PubMed
description A small library of 3-hydroxyisoindolin-1-ones has been prepared from 3-alkylidenephtalides under ultrasonic irradiation. This practical synthesis is featured by group tolerance, high efficiency and yields. The reaction can also be performed in multigram scale and be further extended to access other motifs of isoindolin-1-ones in a one-pot fashion.
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spelling pubmed-92413592022-07-22 Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives Mardjan, Muhammad Idham Darussalam Hariadi, Muhamad Fadhly Putri, Indah Mutiara Musyarrofah, Nilna Amalia Salimah, Muflihah Priatmoko, Purwono, Bambang Commeiras, Laurent RSC Adv Chemistry A small library of 3-hydroxyisoindolin-1-ones has been prepared from 3-alkylidenephtalides under ultrasonic irradiation. This practical synthesis is featured by group tolerance, high efficiency and yields. The reaction can also be performed in multigram scale and be further extended to access other motifs of isoindolin-1-ones in a one-pot fashion. The Royal Society of Chemistry 2022-06-29 /pmc/articles/PMC9241359/ /pubmed/35873335 http://dx.doi.org/10.1039/d2ra02720h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Mardjan, Muhammad Idham Darussalam
Hariadi, Muhamad Fadhly
Putri, Indah Mutiara
Musyarrofah, Nilna Amalia
Salimah, Muflihah
Priatmoko,
Purwono, Bambang
Commeiras, Laurent
Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives
title Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives
title_full Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives
title_fullStr Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives
title_full_unstemmed Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives
title_short Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives
title_sort ultrasonic-assisted-synthesis of isoindolin-1-one derivatives
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241359/
https://www.ncbi.nlm.nih.gov/pubmed/35873335
http://dx.doi.org/10.1039/d2ra02720h
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