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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Main Authors: Saadia Oubaassine, Angela Köckritz, Reinhard Eckelt, Andreas Martin, Mustapha Ait Ali, Larbi El Firdoussi
Format: Article
Language:English
Published: Wiley 2019-01-01
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.
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institution Kabale University
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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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