Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction
1,3,5-Trisubstituted tetramic acids and 2,3-disubstituted indole derivatives were prepared from β-keto esters derived from amino acids by their reaction with iodophenyl-2-trifluoroacetylamine under Cu-catalysis. Both heterocyclic systems were generated from the same starting materials by choice of t...
| Autores: | , , , |
|---|---|
| Formato: | artículo |
| Fecha de publicación: | 2014 |
| País: | España |
| Recursos: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositorio: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/96241 |
| Acesso em linha: | http://hdl.handle.net/10261/96241 |
| Access Level: | acceso abierto |
| Palavra-chave: | 2,3-Disubstituted indoles Tetramic acids b-Keto esters Amino acids Diversity oriented synthesis |
| id |
ES_809f2a7148f41c9d64d9082fd17c6a28 |
|---|---|
| oai_identifier_str |
oai:digital.csic.es:10261/96241 |
| network_acronym_str |
ES |
| network_name_str |
España |
| repository_id_str |
|
| spelling |
Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reactionGarcía-Aranda, M. IsabelGarcía-López, M. TeresaPérez de Vega, M. JesúsGonzález-Muñiz, Rosario2,3-Disubstituted indolesTetramic acidsb-Keto estersAmino acidsDiversity oriented synthesis1,3,5-Trisubstituted tetramic acids and 2,3-disubstituted indole derivatives were prepared from β-keto esters derived from amino acids by their reaction with iodophenyl-2-trifluoroacetylamine under Cu-catalysis. Both heterocyclic systems were generated from the same starting materials by choice of the appropriate reaction conditions. © 2013 Published by Elsevier Ltd.Peer Reviewed2014201420142014info:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501http://hdl.handle.net/10261/96241reponame:DIGITAL.CSIC. Repositorio Institucional del CSICinstname:Consejo Superior de Investigaciones Científicas (CSIC)Inglésinfo:eu-repo/semantics/openAccessoai:digital.csic.es:10261/962412026-05-22T06:33:51Z |
| dc.title.none.fl_str_mv |
Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction |
| title |
Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction |
| spellingShingle |
Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction García-Aranda, M. Isabel 2,3-Disubstituted indoles Tetramic acids b-Keto esters Amino acids Diversity oriented synthesis |
| title_short |
Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction |
| title_full |
Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction |
| title_fullStr |
Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction |
| title_full_unstemmed |
Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction |
| title_sort |
Tetramic acids and indole derivatives from amino acid β-keto esters. Fine-tuning the conditions of the key Cu-catalyzed reaction |
| dc.creator.none.fl_str_mv |
García-Aranda, M. Isabel García-López, M. Teresa Pérez de Vega, M. Jesús González-Muñiz, Rosario |
| author |
García-Aranda, M. Isabel |
| author_facet |
García-Aranda, M. Isabel García-López, M. Teresa Pérez de Vega, M. Jesús González-Muñiz, Rosario |
| author_role |
author |
| author2 |
García-López, M. Teresa Pérez de Vega, M. Jesús González-Muñiz, Rosario |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
2,3-Disubstituted indoles Tetramic acids b-Keto esters Amino acids Diversity oriented synthesis |
| topic |
2,3-Disubstituted indoles Tetramic acids b-Keto esters Amino acids Diversity oriented synthesis |
| description |
1,3,5-Trisubstituted tetramic acids and 2,3-disubstituted indole derivatives were prepared from β-keto esters derived from amino acids by their reaction with iodophenyl-2-trifluoroacetylamine under Cu-catalysis. Both heterocyclic systems were generated from the same starting materials by choice of the appropriate reaction conditions. © 2013 Published by Elsevier Ltd. |
| publishDate |
2014 |
| dc.date.none.fl_str_mv |
2014 2014 2014 2014 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article http://purl.org/coar/resource_type/c_6501 |
| format |
article |
| dc.identifier.none.fl_str_mv |
http://hdl.handle.net/10261/96241 |
| url |
http://hdl.handle.net/10261/96241 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
| eu_rights_str_mv |
openAccess |
| dc.source.none.fl_str_mv |
reponame:DIGITAL.CSIC. Repositorio Institucional del CSIC instname:Consejo Superior de Investigaciones Científicas (CSIC) |
| instname_str |
Consejo Superior de Investigaciones Científicas (CSIC) |
| reponame_str |
DIGITAL.CSIC. Repositorio Institucional del CSIC |
| collection |
DIGITAL.CSIC. Repositorio Institucional del CSIC |
| repository.name.fl_str_mv |
|
| repository.mail.fl_str_mv |
|
| _version_ |
1869411912017510400 |
| score |
15,811543 |