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 othe...

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Main Authors: Mardjan, Muhammad Idham Darussalam, Hariadi, Muhamad Fadhly, Indah Mutiara Putri, Indah Mutiara, Musyarrofah, Nilna Amalia, Salimah, Muflihah, Purwono, Bambang, Commeiras, Laurent
Format: Other
Language:English
Published: RSC Advances 2022
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Online Access:https://repository.ugm.ac.id/283912/1/Ultrasonicassistedsynthesis-of-isoindolin1one-derivativesRSC-Advances.pdf
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author Mardjan, Muhammad Idham Darussalam
Hariadi, Muhamad Fadhly
Indah Mutiara Putri, Indah Mutiara
Musyarrofah, Nilna Amalia
Salimah, Muflihah
Purwono, Bambang
Commeiras, Laurent
author_facet Mardjan, Muhammad Idham Darussalam
Hariadi, Muhamad Fadhly
Indah Mutiara Putri, Indah Mutiara
Musyarrofah, Nilna Amalia
Salimah, Muflihah
Purwono, Bambang
Commeiras, Laurent
author_sort Mardjan, Muhammad Idham Darussalam
collection UGM
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 oai:generic.eprints.org:2839122023-11-24T09:11:36Z https://repository.ugm.ac.id/283912/ Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives Mardjan, Muhammad Idham Darussalam Hariadi, Muhamad Fadhly Indah Mutiara Putri, Indah Mutiara Musyarrofah, Nilna Amalia Salimah, Muflihah Purwono, Bambang Commeiras, Laurent Organic 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. RSC Advances 2022 Other NonPeerReviewed application/pdf en https://repository.ugm.ac.id/283912/1/Ultrasonicassistedsynthesis-of-isoindolin1one-derivativesRSC-Advances.pdf Mardjan, Muhammad Idham Darussalam and Hariadi, Muhamad Fadhly and Indah Mutiara Putri, Indah Mutiara and Musyarrofah, Nilna Amalia and Salimah, Muflihah and Purwono, Bambang and Commeiras, Laurent (2022) Ultrasonic-assisted-synthesis of isoindolin-1-one derivatives. RSC Advances. https://pubs.rsc.org/en/content/articlelanding/2022/RA/D2RA02720H https://doi.org/10.1039/d2ra02720h
spellingShingle Organic Chemistry
Mardjan, Muhammad Idham Darussalam
Hariadi, Muhamad Fadhly
Indah Mutiara Putri, Indah Mutiara
Musyarrofah, Nilna Amalia
Salimah, Muflihah
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 Organic Chemistry
url https://repository.ugm.ac.id/283912/1/Ultrasonicassistedsynthesis-of-isoindolin1one-derivativesRSC-Advances.pdf
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