Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines

Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines

New diarylquinazolines displaying pharmaceutical potential were synthesized in high yields from 4,7-dichloro-2-(2-methylprop-1-enyl)-6-nitroquinazoline by using microwave-promoted regioselective Suzuki-Miyaura cross-coupling reactions.

Bibliographic Details
Main Authors: Patrice Vanelle, Armand Gellis, Pierre Verhaeghe, Youssef Kabri
Format: Article
Language:English
Published: MDPI AG 2010-04-01
Series:Molecules
Subjects:
quinazoline
Suzuki-Miyaura reaction
microwaves
SRN1
Online Access:http://www.mdpi.com/1420-3049/15/5/2949/
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spelling doaj-e2f3fec234d0426b893630184b9f6bcd2020-11-24T21:04:28ZengMDPI AGMolecules1420-30492010-04-011552949296110.3390/molecules15052949Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-DiarylquinazolinesPatrice VanelleArmand GellisPierre VerhaegheYoussef KabriNew diarylquinazolines displaying pharmaceutical potential were synthesized in high yields from 4,7-dichloro-2-(2-methylprop-1-enyl)-6-nitroquinazoline by using microwave-promoted regioselective Suzuki-Miyaura cross-coupling reactions. http://www.mdpi.com/1420-3049/15/5/2949/quinazolineSuzuki-Miyaura reactionmicrowavesSRN1
collection DOAJ
language English
format Article
sources DOAJ
author Patrice Vanelle
Armand Gellis
Pierre Verhaeghe
Youssef Kabri
spellingShingle Patrice Vanelle
Armand Gellis
Pierre Verhaeghe
Youssef Kabri
Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines
Molecules
quinazoline
Suzuki-Miyaura reaction
microwaves
SRN1
author_facet Patrice Vanelle
Armand Gellis
Pierre Verhaeghe
Youssef Kabri
author_sort Patrice Vanelle
title Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines
title_short Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines
title_full Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines
title_fullStr Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines
title_full_unstemmed Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines
title_sort regioselective suzuki-miyaura reaction: application to the microwave-promoted synthesis of 4,7-diarylquinazolines
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2010-04-01
description New diarylquinazolines displaying pharmaceutical potential were synthesized in high yields from 4,7-dichloro-2-(2-methylprop-1-enyl)-6-nitroquinazoline by using microwave-promoted regioselective Suzuki-Miyaura cross-coupling reactions.
topic quinazoline
Suzuki-Miyaura reaction
microwaves
SRN1
url http://www.mdpi.com/1420-3049/15/5/2949/
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AT armandgellis regioselectivesuzukimiyaurareactionapplicationtothemicrowavepromotedsynthesisof47diarylquinazolines
AT pierreverhaeghe regioselectivesuzukimiyaurareactionapplicationtothemicrowavepromotedsynthesisof47diarylquinazolines
AT youssefkabri regioselectivesuzukimiyaurareactionapplicationtothemicrowavepromotedsynthesisof47diarylquinazolines
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