Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction
New hexacyclo and octacyclo compounds have been synthesized by a short route whose key step consists of a single or double domino nucleophilic substitution of neopentyl‐type iodides with potassium cyclopentadienide, followed by intramolecular Diels-Alder cycloaddition.
| Autores: | , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2015 |
| País: | España |
| Institución: | Universidad de Barcelona |
| Repositorio: | Dipòsit Digital de la UB |
| OAI Identifier: | oai:diposit.ub.edu:2445/164843 |
| Acceso en línea: | https://hdl.handle.net/2445/164843 |
| Access Level: | acceso abierto |
| Palabra clave: | Reacció de Diels-Alder Diels-Alder reaction |
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Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reactionCamps García, PelayoLozano Mena, DavidFont Bardia, Ma. MercedesReacció de Diels-AlderDiels-Alder reactionNew hexacyclo and octacyclo compounds have been synthesized by a short route whose key step consists of a single or double domino nucleophilic substitution of neopentyl‐type iodides with potassium cyclopentadienide, followed by intramolecular Diels-Alder cycloaddition.Wiley-VCH2015info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionapplication/pdfhttps://hdl.handle.net/2445/164843Articles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)reponame:Dipòsit Digital de la UBinstname:Universidad de BarcelonaInglésVersió postprint del document publicat a: https://doi.org/10.1002/ejoc.201500601European Journal of Organic Chemistry, 2015, vol. 2015, num. 22, p. 5013-5020https://doi.org/10.1002/ejoc.201500601(c) Wiley-VCH, 2015info:eu-repo/semantics/openAccessoai:diposit.ub.edu:2445/1648432026-05-27T06:46:51Z |
| dc.title.none.fl_str_mv |
Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction |
| title |
Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction |
| spellingShingle |
Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction Camps García, Pelayo Reacció de Diels-Alder Diels-Alder reaction |
| title_short |
Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction |
| title_full |
Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction |
| title_fullStr |
Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction |
| title_full_unstemmed |
Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction |
| title_sort |
Synthesis of polycycles by single or double domino nucleophilic substitution. Diels-Alder reaction |
| dc.creator.none.fl_str_mv |
Camps García, Pelayo Lozano Mena, David Font Bardia, Ma. Mercedes |
| author |
Camps García, Pelayo |
| author_facet |
Camps García, Pelayo Lozano Mena, David Font Bardia, Ma. Mercedes |
| author_role |
author |
| author2 |
Lozano Mena, David Font Bardia, Ma. Mercedes |
| author2_role |
author author |
| dc.subject.none.fl_str_mv |
Reacció de Diels-Alder Diels-Alder reaction |
| topic |
Reacció de Diels-Alder Diels-Alder reaction |
| description |
New hexacyclo and octacyclo compounds have been synthesized by a short route whose key step consists of a single or double domino nucleophilic substitution of neopentyl‐type iodides with potassium cyclopentadienide, followed by intramolecular Diels-Alder cycloaddition. |
| publishDate |
2015 |
| dc.date.none.fl_str_mv |
2015 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion |
| format |
article |
| status_str |
acceptedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/164843 |
| url |
https://hdl.handle.net/2445/164843 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Versió postprint del document publicat a: https://doi.org/10.1002/ejoc.201500601 European Journal of Organic Chemistry, 2015, vol. 2015, num. 22, p. 5013-5020 https://doi.org/10.1002/ejoc.201500601 |
| dc.rights.none.fl_str_mv |
(c) Wiley-VCH, 2015 info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
(c) Wiley-VCH, 2015 |
| eu_rights_str_mv |
openAccess |
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application/pdf |
| dc.publisher.none.fl_str_mv |
Wiley-VCH |
| publisher.none.fl_str_mv |
Wiley-VCH |
| dc.source.none.fl_str_mv |
Articles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada) reponame:Dipòsit Digital de la UB instname:Universidad de Barcelona |
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Universidad de Barcelona |
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Dipòsit Digital de la UB |
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Dipòsit Digital de la UB |
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15,300724 |