Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides
In a one-step procedure, various β-bromoalcohols were synthesized from natural terpenes in good to excellent yields. Using different catalysts, the reaction was carried out at room temperature, with H2O as nucleophile and N-bromosuccinimide as a bromine source under mild reaction conditions. The syn...
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Format: | Article |
Language: | English |
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Wiley
2019-01-01
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Series: | Journal of Chemistry |
Online Access: | http://dx.doi.org/10.1155/2019/9268567 |
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author | Saadia Oubaassine Angela Köckritz Reinhard Eckelt Andreas Martin Mustapha Ait Ali Larbi El Firdoussi |
author_facet | Saadia Oubaassine Angela Köckritz Reinhard Eckelt Andreas Martin Mustapha Ait Ali Larbi El Firdoussi |
author_sort | Saadia Oubaassine |
collection | DOAJ |
description | In a one-step procedure, various β-bromoalcohols were synthesized from natural terpenes in good to excellent yields. Using different catalysts, the reaction was carried out at room temperature, with H2O as nucleophile and N-bromosuccinimide as a bromine source under mild reaction conditions. The synthesized β-bromoalcohols were subsequently converted in situ to the corresponding epoxides in good yields. |
format | Article |
id | doaj-art-9fbd98611faf4fa0a3a858bc263c46e1 |
institution | Kabale University |
issn | 2090-9063 2090-9071 |
language | English |
publishDate | 2019-01-01 |
publisher | Wiley |
record_format | Article |
series | Journal of Chemistry |
spelling | doaj-art-9fbd98611faf4fa0a3a858bc263c46e12025-02-03T05:59:51ZengWileyJournal of Chemistry2090-90632090-90712019-01-01201910.1155/2019/92685679268567Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic EpoxidesSaadia Oubaassine0Angela Köckritz1Reinhard Eckelt2Andreas Martin3Mustapha Ait Ali4Larbi El Firdoussi5Leibniz-Institut für Katalyse e. V. (LIKAT Rostock), Albert-Einstein-Str. 29 a, 18059 Rostock, GermanyLeibniz-Institut für Katalyse e. V. (LIKAT Rostock), Albert-Einstein-Str. 29 a, 18059 Rostock, GermanyLeibniz-Institut für Katalyse e. V. (LIKAT Rostock), Albert-Einstein-Str. 29 a, 18059 Rostock, GermanyLeibniz-Institut für Katalyse e. V. (LIKAT Rostock), Albert-Einstein-Str. 29 a, 18059 Rostock, GermanyDepartment of Chemistry, Equipe de Chimie de Coordination et Catalyse, Faculty of Sciences Semlalia, Cadi Ayyad University, P.O. Box: 2390, 40001 Marrakech, MoroccoDepartment of Chemistry, Equipe de Chimie de Coordination et Catalyse, Faculty of Sciences Semlalia, Cadi Ayyad University, P.O. Box: 2390, 40001 Marrakech, MoroccoIn a one-step procedure, various β-bromoalcohols were synthesized from natural terpenes in good to excellent yields. Using different catalysts, the reaction was carried out at room temperature, with H2O as nucleophile and N-bromosuccinimide as a bromine source under mild reaction conditions. The synthesized β-bromoalcohols were subsequently converted in situ to the corresponding epoxides in good yields.http://dx.doi.org/10.1155/2019/9268567 |
spellingShingle | Saadia Oubaassine Angela Köckritz Reinhard Eckelt Andreas Martin Mustapha Ait Ali Larbi El Firdoussi Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides Journal of Chemistry |
title | Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_full | Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_fullStr | Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_full_unstemmed | Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_short | Catalytic β-Bromohydroxylation of Natural Terpenes: Useful Intermediates for the Synthesis of Terpenic Epoxides |
title_sort | catalytic β bromohydroxylation of natural terpenes useful intermediates for the synthesis of terpenic epoxides |
url | http://dx.doi.org/10.1155/2019/9268567 |
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