<b>Solvent-free synthesis of xanthene derivatives by Preyssler type heteropolyacid</b>
Dimedone reacted with aromatic aldehydes and 3,4-methylenedioxyphenol or β-naphthol in the presence of a catalytic amount of Preyssler type heteropolyacid, H<sub>14</sub>[NaP<sub>5</sub>W<sub>30</sub>O<sub>110</sub>], as a green and reusable catalyst u...
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Format: | Article |
Language: | English |
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Chemical Society of Ethiopia
2011-12-01
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Series: | Bulletin of the Chemical Society of Ethiopia |
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Online Access: | http://ajol.info/index.php/bcse/article/view/68592 |
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author | Fatemeh F. Bamoharram Hossein A. Oskooie Mina Saeedi Khadijeh Bakhtiari Hamideh Alinejhad Majid M. Heravi |
author_facet | Fatemeh F. Bamoharram Hossein A. Oskooie Mina Saeedi Khadijeh Bakhtiari Hamideh Alinejhad Majid M. Heravi |
author_sort | Fatemeh F. Bamoharram |
collection | DOAJ |
description | Dimedone reacted with aromatic aldehydes and 3,4-methylenedioxyphenol or β-naphthol in the presence of a catalytic amount of Preyssler type heteropolyacid, H<sub>14</sub>[NaP<sub>5</sub>W<sub>30</sub>O<sub>110</sub>], as a green and reusable catalyst under solvent-free conditions to form a variety of new xanthene derivatives in very good yields. |
first_indexed | 2024-12-11T08:35:35Z |
format | Article |
id | doaj.art-bffa43cf977d4829beeeeb24c30306a6 |
institution | Directory Open Access Journal |
issn | 1011-3924 1726-801X |
language | English |
last_indexed | 2024-12-11T08:35:35Z |
publishDate | 2011-12-01 |
publisher | Chemical Society of Ethiopia |
record_format | Article |
series | Bulletin of the Chemical Society of Ethiopia |
spelling | doaj.art-bffa43cf977d4829beeeeb24c30306a62022-12-22T01:14:21ZengChemical Society of EthiopiaBulletin of the Chemical Society of Ethiopia1011-39241726-801X2011-12-01253399406<b>Solvent-free synthesis of xanthene derivatives by Preyssler type heteropolyacid</b>Fatemeh F. BamoharramHossein A. OskooieMina SaeediKhadijeh BakhtiariHamideh AlinejhadMajid M. HeraviDimedone reacted with aromatic aldehydes and 3,4-methylenedioxyphenol or β-naphthol in the presence of a catalytic amount of Preyssler type heteropolyacid, H<sub>14</sub>[NaP<sub>5</sub>W<sub>30</sub>O<sub>110</sub>], as a green and reusable catalyst under solvent-free conditions to form a variety of new xanthene derivatives in very good yields.http://ajol.info/index.php/bcse/article/view/68592Xanthene derivativesSolvent-free synthesisPreyssler type heteropolyacid34-Methylene dioxyphenolβ -NaphtholThree-component one-pot reactions |
spellingShingle | Fatemeh F. Bamoharram Hossein A. Oskooie Mina Saeedi Khadijeh Bakhtiari Hamideh Alinejhad Majid M. Heravi <b>Solvent-free synthesis of xanthene derivatives by Preyssler type heteropolyacid</b> Bulletin of the Chemical Society of Ethiopia Xanthene derivatives Solvent-free synthesis Preyssler type heteropolyacid 3 4-Methylene dioxyphenol β -Naphthol Three-component one-pot reactions |
title | <b>Solvent-free synthesis of xanthene derivatives by Preyssler type heteropolyacid</b> |
title_full | <b>Solvent-free synthesis of xanthene derivatives by Preyssler type heteropolyacid</b> |
title_fullStr | <b>Solvent-free synthesis of xanthene derivatives by Preyssler type heteropolyacid</b> |
title_full_unstemmed | <b>Solvent-free synthesis of xanthene derivatives by Preyssler type heteropolyacid</b> |
title_short | <b>Solvent-free synthesis of xanthene derivatives by Preyssler type heteropolyacid</b> |
title_sort | b solvent free synthesis of xanthene derivatives by preyssler type heteropolyacid b |
topic | Xanthene derivatives Solvent-free synthesis Preyssler type heteropolyacid 3 4-Methylene dioxyphenol β -Naphthol Three-component one-pot reactions |
url | http://ajol.info/index.php/bcse/article/view/68592 |
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