Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives
Producción Científica
| Autores: | , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión aceptada para publicación |
| Fecha de publicación: | 2019 |
| País: | España |
| Institución: | Universidad de Valladolid |
| Repositorio: | UVaDOC. Repositorio Documental de la Universidad de Valladolid |
| OAI Identifier: | oai:uvadoc.uva.es:10324/38103 |
| Acceso en línea: | https://doi.org/10.1002/adsc.201801454 http://uvadoc.uva.es/handle/10324/38103 |
| Access Level: | acceso abierto |
| Palabra clave: | Síntesis asimétrica Metátesis Asymmetric synthesis Metathesis |
| id |
ES_fc7030fa15a4a8b37b1e547b9c8fa41f |
|---|---|
| oai_identifier_str |
oai:uvadoc.uva.es:10324/38103 |
| network_acronym_str |
ES |
| network_name_str |
España |
| repository_id_str |
|
| spelling |
Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine DerivativesGutiérrez Loriente, AgustínMartín Álvarez, José MiguelPrieto, ElenaAndrés Juan, CeliaNieto Román, Francisco JavierSíntesis asimétricaMetátesisAsymmetric synthesisMetathesisProducción CientíficaDiastereoselective ring‐closing metathesis reactions on chiral trienic perhydro‐1,3‐benzoxazines derived from (−)‐8‐aminomenthol featuring two diastereotopic olefin chains is described. The diastereochemical outcome of the cyclization appeared to be dependent on the length and position of the olefin chains in perhydro‐1,3‐benzoxazine, the degree of substitution of the double bonds and the ruthenium catalyst used. After separation of the diastereomers, and removal of the chiral auxiliary, enantiopure oxygen‐ and nitrogen‐containing heterocycles were obtained.Ministerio de Economía, Industria y Competitividad (Project FEDER-CTQ2014-59870-P)Junta de Castilla y León (Ref. Project FEDER-VA115P17)Wiley2019info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersionapplication/pdfhttps://doi.org/10.1002/adsc.201801454http://uvadoc.uva.es/handle/10324/38103reponame:UVaDOC. Repositorio Documental de la Universidad de Valladolidinstname:Universidad de ValladolidIngléshttps://onlinelibrary.wiley.com/doi/10.1002/adsc.201801454info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/4.0/oai:uvadoc.uva.es:10324/381032026-06-13T12:44:47Z |
| dc.title.none.fl_str_mv |
Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives |
| title |
Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives |
| spellingShingle |
Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives Gutiérrez Loriente, Agustín Síntesis asimétrica Metátesis Asymmetric synthesis Metathesis |
| title_short |
Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives |
| title_full |
Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives |
| title_fullStr |
Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives |
| title_full_unstemmed |
Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives |
| title_sort |
Synthesis of Enantiopure Oxygen- and Nitrogen-Containing Heterocycles by Diastereoselective Ring-Closing Metathesis Reaction in Perhydro-1,3-benzoxazine Derivatives |
| dc.creator.none.fl_str_mv |
Gutiérrez Loriente, Agustín Martín Álvarez, José Miguel Prieto, Elena Andrés Juan, Celia Nieto Román, Francisco Javier |
| author |
Gutiérrez Loriente, Agustín |
| author_facet |
Gutiérrez Loriente, Agustín Martín Álvarez, José Miguel Prieto, Elena Andrés Juan, Celia Nieto Román, Francisco Javier |
| author_role |
author |
| author2 |
Martín Álvarez, José Miguel Prieto, Elena Andrés Juan, Celia Nieto Román, Francisco Javier |
| author2_role |
author author author author |
| dc.subject.none.fl_str_mv |
Síntesis asimétrica Metátesis Asymmetric synthesis Metathesis |
| topic |
Síntesis asimétrica Metátesis Asymmetric synthesis Metathesis |
| description |
Producción Científica |
| publishDate |
2019 |
| dc.date.none.fl_str_mv |
2019 |
| 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://doi.org/10.1002/adsc.201801454 http://uvadoc.uva.es/handle/10324/38103 |
| url |
https://doi.org/10.1002/adsc.201801454 http://uvadoc.uva.es/handle/10324/38103 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
https://onlinelibrary.wiley.com/doi/10.1002/adsc.201801454 |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| eu_rights_str_mv |
openAccess |
| rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| dc.format.none.fl_str_mv |
application/pdf |
| dc.publisher.none.fl_str_mv |
Wiley |
| publisher.none.fl_str_mv |
Wiley |
| dc.source.none.fl_str_mv |
reponame:UVaDOC. Repositorio Documental de la Universidad de Valladolid instname:Universidad de Valladolid |
| instname_str |
Universidad de Valladolid |
| reponame_str |
UVaDOC. Repositorio Documental de la Universidad de Valladolid |
| collection |
UVaDOC. Repositorio Documental de la Universidad de Valladolid |
| repository.name.fl_str_mv |
|
| repository.mail.fl_str_mv |
|
| _version_ |
1869425422449508352 |
| score |
15.301603 |