Catalytic Synthesis and Antifungal Activity of New Polychlorinated Natural Terpenes
Various unsaturated natural terpenes were selectively converted to the corresponding polychlorinated products in good yields using iron acetylacetonate in combination with nucleophilic cocatalyst. The synthesized compounds were evaluated for their in vitro antifungal activity. The antifungal bioassa...
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Format: | Article |
Language: | English |
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Wiley
2017-01-01
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Series: | Advances in Materials Science and Engineering |
Online Access: | http://dx.doi.org/10.1155/2017/2784303 |
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author | Hana Ighachane Brahim Boualy Mustapha Ait Ali My. H. Sedra Larbi El Firdoussi Hassan Bihi Lazrek |
author_facet | Hana Ighachane Brahim Boualy Mustapha Ait Ali My. H. Sedra Larbi El Firdoussi Hassan Bihi Lazrek |
author_sort | Hana Ighachane |
collection | DOAJ |
description | Various unsaturated natural terpenes were selectively converted to the corresponding polychlorinated products in good yields using iron acetylacetonate in combination with nucleophilic cocatalyst. The synthesized compounds were evaluated for their in vitro antifungal activity. The antifungal bioassays showed that 2c and 2d possessed significant antifungal activity against Fusarium oxysporum f. sp. albedinis (Foa), Fusarium oxysporum f. sp. canariensis (Foc), and Verticillium dahliae (Vd). |
format | Article |
id | doaj-art-4b03f17e271a456685b396b257d86b3d |
institution | Kabale University |
issn | 1687-8434 1687-8442 |
language | English |
publishDate | 2017-01-01 |
publisher | Wiley |
record_format | Article |
series | Advances in Materials Science and Engineering |
spelling | doaj-art-4b03f17e271a456685b396b257d86b3d2025-02-03T06:00:44ZengWileyAdvances in Materials Science and Engineering1687-84341687-84422017-01-01201710.1155/2017/27843032784303Catalytic Synthesis and Antifungal Activity of New Polychlorinated Natural TerpenesHana Ighachane0Brahim Boualy1Mustapha Ait Ali2My. H. Sedra3Larbi El Firdoussi4Hassan Bihi Lazrek5Laboratory of Biomolecular and Medicinal Chemistry, URAC 16, Faculty of Sciences Semlalia, Marrakech, MoroccoLaboratoire de Chimie et Modélisation Mathématique, Faculté Polydisciplinaire de Khouribga, Université Hassan 1er, BP 145, 25000 Khouribga, MoroccoEquipe de Chimie de Coordination et Catalyse, Département de Chimie, Faculté des Sciences Semlalia, Université Cadi Ayyad, BP 2390, 40001 Marrakech, MoroccoLaboratory of Biomolecular and Medicinal Chemistry, URAC 16, Faculty of Sciences Semlalia, Marrakech, MoroccoEquipe de Chimie de Coordination et Catalyse, Département de Chimie, Faculté des Sciences Semlalia, Université Cadi Ayyad, BP 2390, 40001 Marrakech, MoroccoLaboratory of Biomolecular and Medicinal Chemistry, URAC 16, Faculty of Sciences Semlalia, Marrakech, MoroccoVarious unsaturated natural terpenes were selectively converted to the corresponding polychlorinated products in good yields using iron acetylacetonate in combination with nucleophilic cocatalyst. The synthesized compounds were evaluated for their in vitro antifungal activity. The antifungal bioassays showed that 2c and 2d possessed significant antifungal activity against Fusarium oxysporum f. sp. albedinis (Foa), Fusarium oxysporum f. sp. canariensis (Foc), and Verticillium dahliae (Vd).http://dx.doi.org/10.1155/2017/2784303 |
spellingShingle | Hana Ighachane Brahim Boualy Mustapha Ait Ali My. H. Sedra Larbi El Firdoussi Hassan Bihi Lazrek Catalytic Synthesis and Antifungal Activity of New Polychlorinated Natural Terpenes Advances in Materials Science and Engineering |
title | Catalytic Synthesis and Antifungal Activity of New Polychlorinated Natural Terpenes |
title_full | Catalytic Synthesis and Antifungal Activity of New Polychlorinated Natural Terpenes |
title_fullStr | Catalytic Synthesis and Antifungal Activity of New Polychlorinated Natural Terpenes |
title_full_unstemmed | Catalytic Synthesis and Antifungal Activity of New Polychlorinated Natural Terpenes |
title_short | Catalytic Synthesis and Antifungal Activity of New Polychlorinated Natural Terpenes |
title_sort | catalytic synthesis and antifungal activity of new polychlorinated natural terpenes |
url | http://dx.doi.org/10.1155/2017/2784303 |
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