Recent advances in the synthesis of azaphenalene alkaloids
Azaphenalene alkaloids are biosynthesised and segregated by diverse insects of the Coccinellidae family (ladybirds) and are believed to play an important role in the defensive mechanism against their natural predators. The particular unique framework of these alkaloids, along with their potential in...
| Autores: | , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2018 |
| País: | España |
| Institución: | Universitat Autònoma de Barcelona |
| Repositorio: | Dipòsit Digital de Documents de la UAB |
| Idioma: | inglés |
| OAI Identifier: | oai:ddd.uab.cat:195986 |
| Acceso en línea: | https://ddd.uab.cat/record/195986 https://dx.doi.org/urn:doi:10.1039/c8ob01443d |
| Access Level: | acceso abierto |
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Recent advances in the synthesis of azaphenalene alkaloidsfirst enantioselective approachesAlujas Burgos, SílviaBayón, Pau|||0000-0002-3064-8866Figueredo Galimany, Marta|||0000-0002-8278-7534Azaphenalene alkaloids are biosynthesised and segregated by diverse insects of the Coccinellidae family (ladybirds) and are believed to play an important role in the defensive mechanism against their natural predators. The particular unique framework of these alkaloids, along with their potential in the field of biological pest control, has led to several research groups developing synthetic sequences to prepare these compounds. The main purpose of the present review is to provide an update of the more recent synthetic progress towards these alkaloids, including the pioneering enantioselective approaches to chiral congeners. 22018-01-0120182018-01-01Articlehttp://purl.org/coar/resource_type/c_6501AMhttp://purl.org/coar/version/c_ab4af688f83e57aainfo:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/195986https://dx.doi.org/urn:doi:10.1039/c8ob01443dreponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengMinisterio de Economía y Competitividad https://doi.org/10.13039/501100003329 CTQ2013-41161-RMinisterio de Ciencia e Innovación https://doi.org/10.13039/501100004837 CTQ2010-15380open accesshttp://purl.org/coar/access_right/c_abf2Aquest material està protegit per drets d'autor i/o drets afins. Podeu utilitzar aquest material en funció del que permet la legislació de drets d'autor i drets afins d'aplicació al vostre cas. Per a d'altres usos heu d'obtenir permís del(s) titular(s) de drets.https://rightsstatements.org/vocab/InC/1.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:1959862026-06-06T12:50:31Z |
| dc.title.none.fl_str_mv |
Recent advances in the synthesis of azaphenalene alkaloids first enantioselective approaches |
| title |
Recent advances in the synthesis of azaphenalene alkaloids |
| spellingShingle |
Recent advances in the synthesis of azaphenalene alkaloids Alujas Burgos, Sílvia |
| title_short |
Recent advances in the synthesis of azaphenalene alkaloids |
| title_full |
Recent advances in the synthesis of azaphenalene alkaloids |
| title_fullStr |
Recent advances in the synthesis of azaphenalene alkaloids |
| title_full_unstemmed |
Recent advances in the synthesis of azaphenalene alkaloids |
| title_sort |
Recent advances in the synthesis of azaphenalene alkaloids |
| dc.creator.none.fl_str_mv |
Alujas Burgos, Sílvia Bayón, Pau|||0000-0002-3064-8866 Figueredo Galimany, Marta|||0000-0002-8278-7534 |
| author |
Alujas Burgos, Sílvia |
| author_facet |
Alujas Burgos, Sílvia Bayón, Pau|||0000-0002-3064-8866 Figueredo Galimany, Marta|||0000-0002-8278-7534 |
| author_role |
author |
| author2 |
Bayón, Pau|||0000-0002-3064-8866 Figueredo Galimany, Marta|||0000-0002-8278-7534 |
| author2_role |
author author |
| description |
Azaphenalene alkaloids are biosynthesised and segregated by diverse insects of the Coccinellidae family (ladybirds) and are believed to play an important role in the defensive mechanism against their natural predators. The particular unique framework of these alkaloids, along with their potential in the field of biological pest control, has led to several research groups developing synthetic sequences to prepare these compounds. The main purpose of the present review is to provide an update of the more recent synthetic progress towards these alkaloids, including the pioneering enantioselective approaches to chiral congeners. |
| publishDate |
2018 |
| dc.date.none.fl_str_mv |
2 2018-01-01 2018 2018-01-01 |
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Article http://purl.org/coar/resource_type/c_6501 AM http://purl.org/coar/version/c_ab4af688f83e57aa |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
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article |
| dc.identifier.none.fl_str_mv |
https://ddd.uab.cat/record/195986 https://dx.doi.org/urn:doi:10.1039/c8ob01443d |
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https://ddd.uab.cat/record/195986 https://dx.doi.org/urn:doi:10.1039/c8ob01443d |
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Inglés eng |
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Inglés |
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eng |
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Ministerio de Economía y Competitividad https://doi.org/10.13039/501100003329 CTQ2013-41161-R Ministerio de Ciencia e Innovación https://doi.org/10.13039/501100004837 CTQ2010-15380 |
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open access http://purl.org/coar/access_right/c_abf2 https://rightsstatements.org/vocab/InC/1.0/ |
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info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 https://rightsstatements.org/vocab/InC/1.0/ |
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openAccess |
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application/pdf |
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reponame:Dipòsit Digital de Documents de la UAB instname:Universitat Autònoma de Barcelona |
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Universitat Autònoma de Barcelona |
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Dipòsit Digital de Documents de la UAB |
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Dipòsit Digital de Documents de la UAB |
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15,300724 |