Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines

Autores
Laha, Joydev K.; Barolo, Silvia Maricel; Rossi, Roberto Arturo; Cuny, Gregory D.
Año de publicación
2011
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
A general synthetic route to prepare all four carboline regioisomers by photostimulated cyclization of anilinohalopyridines is described. The methodology affords various substituted carbolines in good to excellent yields. In the case of α-carbolines, the S(RN)1 methodology complements previously reported palladium-catalyzed cyclization approaches.
Fil: Laha, Joydev K.. Harvard Medical School; Estados Unidos
Fil: Barolo, Silvia Maricel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Rossi, Roberto Arturo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Cuny, Gregory D.. Harvard Medical School; Estados Unidos
Materia
Srn1
Carbolines
Photochemistry
Ring Closure
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/66183
Acceder
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oai_identifier_str oai:ri.conicet.gov.ar:11336/66183
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Synthesis of Carbolines by Photostimulated Cyclization of AnilinohalopyridinesLaha, Joydev K.Barolo, Silvia MaricelRossi, Roberto ArturoCuny, Gregory D.Srn1CarbolinesPhotochemistryRing Closurehttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1A general synthetic route to prepare all four carboline regioisomers by photostimulated cyclization of anilinohalopyridines is described. The methodology affords various substituted carbolines in good to excellent yields. In the case of α-carbolines, the S(RN)1 methodology complements previously reported palladium-catalyzed cyclization approaches.Fil: Laha, Joydev K.. Harvard Medical School; Estados UnidosFil: Barolo, Silvia Maricel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Rossi, Roberto Arturo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Cuny, Gregory D.. Harvard Medical School; Estados UnidosAmerican Chemical Society2011-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/66183Laha, Joydev K.; Barolo, Silvia Maricel; Rossi, Roberto Arturo; Cuny, Gregory D.; Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines; American Chemical Society; Journal of Organic Chemistry; 76; 15; 8-2011; 6421-64250022-32631520-6904CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1021/jo200923ninfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/abs/10.1021/jo200923ninfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:04:41Zoai:ri.conicet.gov.ar:11336/66183instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:04:41.714CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines
title Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines
spellingShingle Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines
Laha, Joydev K.
Srn1
Carbolines
Photochemistry
Ring Closure
title_short Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines
title_full Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines
title_fullStr Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines
title_full_unstemmed Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines
title_sort Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines
dc.creator.none.fl_str_mv Laha, Joydev K.
Barolo, Silvia Maricel
Rossi, Roberto Arturo
Cuny, Gregory D.
author Laha, Joydev K.
author_facet Laha, Joydev K.
Barolo, Silvia Maricel
Rossi, Roberto Arturo
Cuny, Gregory D.
author_role author
author2 Barolo, Silvia Maricel
Rossi, Roberto Arturo
Cuny, Gregory D.
author2_role author
author
author
dc.subject.none.fl_str_mv Srn1
Carbolines
Photochemistry
Ring Closure
topic Srn1
Carbolines
Photochemistry
Ring Closure
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv A general synthetic route to prepare all four carboline regioisomers by photostimulated cyclization of anilinohalopyridines is described. The methodology affords various substituted carbolines in good to excellent yields. In the case of α-carbolines, the S(RN)1 methodology complements previously reported palladium-catalyzed cyclization approaches.
Fil: Laha, Joydev K.. Harvard Medical School; Estados Unidos
Fil: Barolo, Silvia Maricel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Rossi, Roberto Arturo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Cuny, Gregory D.. Harvard Medical School; Estados Unidos
description A general synthetic route to prepare all four carboline regioisomers by photostimulated cyclization of anilinohalopyridines is described. The methodology affords various substituted carbolines in good to excellent yields. In the case of α-carbolines, the S(RN)1 methodology complements previously reported palladium-catalyzed cyclization approaches.
publishDate 2011
dc.date.none.fl_str_mv 2011-08
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/66183
Laha, Joydev K.; Barolo, Silvia Maricel; Rossi, Roberto Arturo; Cuny, Gregory D.; Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines; American Chemical Society; Journal of Organic Chemistry; 76; 15; 8-2011; 6421-6425
0022-3263
1520-6904
CONICET Digital
CONICET
url http://hdl.handle.net/11336/66183
identifier_str_mv Laha, Joydev K.; Barolo, Silvia Maricel; Rossi, Roberto Arturo; Cuny, Gregory D.; Synthesis of Carbolines by Photostimulated Cyclization of Anilinohalopyridines; American Chemical Society; Journal of Organic Chemistry; 76; 15; 8-2011; 6421-6425
0022-3263
1520-6904
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1021/jo200923n
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/abs/10.1021/jo200923n
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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score 13.070432

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