Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)

Autores
Mandal, Debdeep; Chandra, Shubhadeep; Neuman, Nicolás Ignacio; Mahata, Alok; Sarkar, Arighna; Kundu, Abhinanda; Anga, Srinivas; Rawat, Hemant; Schulzke, Carola; Sarkar, Biprajit; Mote, Kaustubh R.; Chandrasekhar, Vadapalli; Jana, Anukul
Año de publicación
2020
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
A N-heterocyclic olefin (NHO), a terminal alkeneselectively activates aromatic C-F bonds without the need of anyadditional catalyst. As a result, a straightforward methodology wasdeveloped for the formation of different fluoroaryl substituted alkenesin which the central carbon-carbon double bond is in a twistedgeometry.
Fil: Mandal, Debdeep. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Chandra, Shubhadeep. Freie Universität Berlin.; Alemania
Fil: Neuman, Nicolás Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina
Fil: Mahata, Alok. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Sarkar, Arighna. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Kundu, Abhinanda. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Anga, Srinivas. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Rawat, Hemant. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Schulzke, Carola. ERNST MORITZ ARNDT UNIVERSITÄT GREIFSWALD (UG);
Fil: Sarkar, Biprajit. Freie Universität Berlin.; Alemania
Fil: Mote, Kaustubh R.. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Chandrasekhar, Vadapalli. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Jana, Anukul. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Materia
N-HETEROCYCLIC OLEFIN
C-F BOND ACTIVATION
METAL-FREE
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:11336/107026
Acceder
id CONICETDig_2ad0fd69bfde95a79ac75ad60dcf50ba
oai_identifier_str oai:ri.conicet.gov.ar:11336/107026
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)Mandal, DebdeepChandra, ShubhadeepNeuman, Nicolás IgnacioMahata, AlokSarkar, ArighnaKundu, AbhinandaAnga, SrinivasRawat, HemantSchulzke, CarolaSarkar, BiprajitMote, Kaustubh R.Chandrasekhar, VadapalliJana, AnukulN-HETEROCYCLIC OLEFINC-F BOND ACTIVATIONMETAL-FREEhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1A N-heterocyclic olefin (NHO), a terminal alkeneselectively activates aromatic C-F bonds without the need of anyadditional catalyst. As a result, a straightforward methodology wasdeveloped for the formation of different fluoroaryl substituted alkenesin which the central carbon-carbon double bond is in a twistedgeometry.Fil: Mandal, Debdeep. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; EspañaFil: Chandra, Shubhadeep. Freie Universität Berlin.; AlemaniaFil: Neuman, Nicolás Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; ArgentinaFil: Mahata, Alok. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; EspañaFil: Sarkar, Arighna. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; EspañaFil: Kundu, Abhinanda. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; EspañaFil: Anga, Srinivas. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; EspañaFil: Rawat, Hemant. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; EspañaFil: Schulzke, Carola. ERNST MORITZ ARNDT UNIVERSITÄT GREIFSWALD (UG); Fil: Sarkar, Biprajit. Freie Universität Berlin.; AlemaniaFil: Mote, Kaustubh R.. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; EspañaFil: Chandrasekhar, Vadapalli. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; EspañaFil: Jana, Anukul. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; EspañaWiley VCH Verlag2020-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/107026Mandal, Debdeep; Chandra, Shubhadeep; Neuman, Nicolás Ignacio; Mahata, Alok; Sarkar, Arighna; et al.; Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO); Wiley VCH Verlag; Chemistry- A European Journal; 2-20200947-6539CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202000276info:eu-repo/semantics/altIdentifier/doi/10.1002/chem.202000276info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:04:33Zoai:ri.conicet.gov.ar:11336/107026instacron: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 10:04:33.568CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)
title Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)
spellingShingle Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)
Mandal, Debdeep
N-HETEROCYCLIC OLEFIN
C-F BOND ACTIVATION
METAL-FREE
title_short Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)
title_full Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)
title_fullStr Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)
title_full_unstemmed Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)
title_sort Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO)
dc.creator.none.fl_str_mv Mandal, Debdeep
Chandra, Shubhadeep
Neuman, Nicolás Ignacio
Mahata, Alok
Sarkar, Arighna
Kundu, Abhinanda
Anga, Srinivas
Rawat, Hemant
Schulzke, Carola
Sarkar, Biprajit
Mote, Kaustubh R.
Chandrasekhar, Vadapalli
Jana, Anukul
author Mandal, Debdeep
author_facet Mandal, Debdeep
Chandra, Shubhadeep
Neuman, Nicolás Ignacio
Mahata, Alok
Sarkar, Arighna
Kundu, Abhinanda
Anga, Srinivas
Rawat, Hemant
Schulzke, Carola
Sarkar, Biprajit
Mote, Kaustubh R.
Chandrasekhar, Vadapalli
Jana, Anukul
author_role author
author2 Chandra, Shubhadeep
Neuman, Nicolás Ignacio
Mahata, Alok
Sarkar, Arighna
Kundu, Abhinanda
Anga, Srinivas
Rawat, Hemant
Schulzke, Carola
Sarkar, Biprajit
Mote, Kaustubh R.
Chandrasekhar, Vadapalli
Jana, Anukul
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv N-HETEROCYCLIC OLEFIN
C-F BOND ACTIVATION
METAL-FREE
topic N-HETEROCYCLIC OLEFIN
C-F BOND ACTIVATION
METAL-FREE
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 N-heterocyclic olefin (NHO), a terminal alkeneselectively activates aromatic C-F bonds without the need of anyadditional catalyst. As a result, a straightforward methodology wasdeveloped for the formation of different fluoroaryl substituted alkenesin which the central carbon-carbon double bond is in a twistedgeometry.
Fil: Mandal, Debdeep. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Chandra, Shubhadeep. Freie Universität Berlin.; Alemania
Fil: Neuman, Nicolás Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Desarrollo Tecnológico para la Industria Química. Universidad Nacional del Litoral. Instituto de Desarrollo Tecnológico para la Industria Química; Argentina
Fil: Mahata, Alok. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Sarkar, Arighna. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Kundu, Abhinanda. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Anga, Srinivas. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Rawat, Hemant. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Schulzke, Carola. ERNST MORITZ ARNDT UNIVERSITÄT GREIFSWALD (UG);
Fil: Sarkar, Biprajit. Freie Universität Berlin.; Alemania
Fil: Mote, Kaustubh R.. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Chandrasekhar, Vadapalli. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
Fil: Jana, Anukul. International Centre Of Theoretical Science. Tata Institute Of Fundamental Research; España
description A N-heterocyclic olefin (NHO), a terminal alkeneselectively activates aromatic C-F bonds without the need of anyadditional catalyst. As a result, a straightforward methodology wasdeveloped for the formation of different fluoroaryl substituted alkenesin which the central carbon-carbon double bond is in a twistedgeometry.
publishDate 2020
dc.date.none.fl_str_mv 2020-02
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/11336/107026
Mandal, Debdeep; Chandra, Shubhadeep; Neuman, Nicolás Ignacio; Mahata, Alok; Sarkar, Arighna; et al.; Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO); Wiley VCH Verlag; Chemistry- A European Journal; 2-2020
0947-6539
CONICET Digital
CONICET
url http://hdl.handle.net/11336/107026
identifier_str_mv Mandal, Debdeep; Chandra, Shubhadeep; Neuman, Nicolás Ignacio; Mahata, Alok; Sarkar, Arighna; et al.; Activation of Aromatic C‐F Bonds by a N‐Heterocyclic Olefin (NHO); Wiley VCH Verlag; Chemistry- A European Journal; 2-2020
0947-6539
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202000276
info:eu-repo/semantics/altIdentifier/doi/10.1002/chem.202000276
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
dc.publisher.none.fl_str_mv Wiley VCH Verlag
publisher.none.fl_str_mv Wiley VCH Verlag
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
_version_ 1844613872724475904
score 13.070432

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