Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds

Throughout the history of synthetic chemistry, the pursuit of more efficient and sustainable processes has become progressively significant. Modern organic synthesis not only seeks the preparation of target molecules but also designing processes that maximize resource efficiency. This involves conse...

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Bibliographic Details
Author: Arribas Domingo, Andrés
Format: doctoral thesis
Publication Date:2025
Country:España
Institution:Universidad de Santiago de Compostela (USC)
Repository:Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
Language:English
OAI Identifier:oai:dnet:minerva_____::2b2063bb81ae716ff968ea10a4ec3286
Online Access:https://hdl.handle.net/10347/41032
Access Level:Open access
Keyword:iridium
catalysis
hydroarylation
C-H activation
enantioselective
230615 Mecanismos de reacción
230610 Compuestos heterocíclicos
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spelling Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic ScaffoldsArribas Domingo, AndrésiridiumcatalysishydroarylationC-H activationenantioselective230615 Mecanismos de reacción230610 Compuestos heterocíclicosThroughout the history of synthetic chemistry, the pursuit of more efficient and sustainable processes has become progressively significant. Modern organic synthesis not only seeks the preparation of target molecules but also designing processes that maximize resource efficiency. This involves conserving the maximum number of atoms from starting materials (atom economy), reducing the number of synthetic steps (step economy), and minimizing the need for intermediate purification (pot economy).López García, Fernando JoséMascareñas Cid, José LuisUniversidade de Santiago de Compostela. Escola de Doutoramento Internacional (EDIUS)20252025-01-0120252025-01-01doctoral thesishttp://purl.org/coar/resource_type/c_db06info:eu-repo/semantics/doctoralThesisapplication/pdfhttps://hdl.handle.net/10347/41032reponame:Minerva. Repositorio Institucional de la Universidad de Santiago de Compostelainstname:Universidad de Santiago de Compostela (USC)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2Attribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessoai:dnet:minerva_____::2b2063bb81ae716ff968ea10a4ec32862026-06-15T12:47:27Z
dc.title.none.fl_str_mv Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds
title Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds
spellingShingle Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds
Arribas Domingo, Andrés
iridium
catalysis
hydroarylation
C-H activation
enantioselective
230615 Mecanismos de reacción
230610 Compuestos heterocíclicos
title_short Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds
title_full Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds
title_fullStr Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds
title_full_unstemmed Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds
title_sort Iridium-Catalyzed Hydrocarbonation of Unsaturated Systems: Enantioselective Synthesis of Heteropolycyclic Scaffolds
dc.creator.none.fl_str_mv Arribas Domingo, Andrés
author Arribas Domingo, Andrés
author_facet Arribas Domingo, Andrés
author_role author
dc.contributor.none.fl_str_mv López García, Fernando José
Mascareñas Cid, José Luis
Universidade de Santiago de Compostela. Escola de Doutoramento Internacional (EDIUS)

dc.subject.none.fl_str_mv iridium
catalysis
hydroarylation
C-H activation
enantioselective
230615 Mecanismos de reacción
230610 Compuestos heterocíclicos
topic iridium
catalysis
hydroarylation
C-H activation
enantioselective
230615 Mecanismos de reacción
230610 Compuestos heterocíclicos
description Throughout the history of synthetic chemistry, the pursuit of more efficient and sustainable processes has become progressively significant. Modern organic synthesis not only seeks the preparation of target molecules but also designing processes that maximize resource efficiency. This involves conserving the maximum number of atoms from starting materials (atom economy), reducing the number of synthetic steps (step economy), and minimizing the need for intermediate purification (pot economy).
publishDate 2025
dc.date.none.fl_str_mv 2025
2025-01-01
2025
2025-01-01
dc.type.none.fl_str_mv doctoral thesis
http://purl.org/coar/resource_type/c_db06
dc.type.openaire.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
dc.identifier.none.fl_str_mv https://hdl.handle.net/10347/41032
url https://hdl.handle.net/10347/41032
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
Attribution-NonCommercial-NoDerivatives 4.0 International
http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname:Universidad de Santiago de Compostela (USC)
instname_str Universidad de Santiago de Compostela (USC)
reponame_str Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
collection Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
repository.name.fl_str_mv
repository.mail.fl_str_mv
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