Advances in the synthesis of 5-and 6-substituted uracil derivatives

Autores
Bardagi, Javier Ivan; Rossi, Roberto Arturo
Año de publicación
2009
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The uracil unit is one of the most important structures in life, it being part of the building blocks of RNA and DNA and other natural products; therefore, it is not surprising that uracil derivatives have important biological activity. Uracil-based compounds are used in the treatment of cancer (5-fluoruracil) and against infections of the HIV virus (AZT). Actions as antiviral and antitumoral agents are perhaps the most widely reported activity. However, other uracil derivatives have been synthesized which are herbicides, insecticides, bactericides, acaricides, etc. In addition, uracil units can be found in the chemistry of peptide nucleic acid (PNA) or as part of other fused systems with antiallergic, antihypertensive, cardiotonic, bronchodilator or antibronchitis activity.The search for uracil derivatives has been carried out since the beginning of the last century and even today there is great interest in the development of new derivatives and strategies for synthesis so as to improve the yield of known compounds. To prepare uracils, there are three main synthetic strategies: a) building the uracil nucleus from acyclic precursors with appropriate substituents; b)modification of the structure of functionalized uracils or uracil itself by reaction with different reagents, as the recent synthesis of 5-trifluoromethyluracil and uridines with oxiranyl and tetrahydrofuranyl substituents; c) functionalization of masked uracil moieties with reactions incompatible with the nucleus, for example the synthesis of 6-aryl and 6- acyluracils and 2 -eoxypseudouridine. Combinations of these approaches are often found in the synthesis of target compounds with potential biological activities.The present review will cover advances in the synthesis of 5- and 6-substituted uracils over the last 8-10 years. This review has been organized in terms of the type of union that links the uracil moieties to the substitution groups; fused systems will have a separate section.
Fil: Bardagi, Javier Ivan. 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
Materia
MINI REVIEW
SYNTHESIS
5- and 6- DERIVATES
URACIL
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:11336/82620

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spelling Advances in the synthesis of 5-and 6-substituted uracil derivativesBardagi, Javier IvanRossi, Roberto ArturoMINI REVIEWSYNTHESIS5- and 6- DERIVATESURACILhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The uracil unit is one of the most important structures in life, it being part of the building blocks of RNA and DNA and other natural products; therefore, it is not surprising that uracil derivatives have important biological activity. Uracil-based compounds are used in the treatment of cancer (5-fluoruracil) and against infections of the HIV virus (AZT). Actions as antiviral and antitumoral agents are perhaps the most widely reported activity. However, other uracil derivatives have been synthesized which are herbicides, insecticides, bactericides, acaricides, etc. In addition, uracil units can be found in the chemistry of peptide nucleic acid (PNA) or as part of other fused systems with antiallergic, antihypertensive, cardiotonic, bronchodilator or antibronchitis activity.The search for uracil derivatives has been carried out since the beginning of the last century and even today there is great interest in the development of new derivatives and strategies for synthesis so as to improve the yield of known compounds. To prepare uracils, there are three main synthetic strategies: a) building the uracil nucleus from acyclic precursors with appropriate substituents; b)modification of the structure of functionalized uracils or uracil itself by reaction with different reagents, as the recent synthesis of 5-trifluoromethyluracil and uridines with oxiranyl and tetrahydrofuranyl substituents; c) functionalization of masked uracil moieties with reactions incompatible with the nucleus, for example the synthesis of 6-aryl and 6- acyluracils and 2 -eoxypseudouridine. Combinations of these approaches are often found in the synthesis of target compounds with potential biological activities.The present review will cover advances in the synthesis of 5- and 6-substituted uracils over the last 8-10 years. This review has been organized in terms of the type of union that links the uracil moieties to the substitution groups; fused systems will have a separate section.Fil: Bardagi, Javier Ivan. 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; ArgentinaRoutledge Journals, Taylor & Francis Ltd2009-01info: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/11336/82620Bardagi, Javier Ivan; Rossi, Roberto Arturo; Advances in the synthesis of 5-and 6-substituted uracil derivatives; Routledge Journals, Taylor & Francis Ltd; Organic Preparations and Procedures International; 41; 6; 1-2009; 479-5140030-49481945-5453CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.tandfonline.com/doi/abs/10.1080/00304940903378776info:eu-repo/semantics/altIdentifier/doi/10.1080/00304940903378776info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:39:39Zoai:ri.conicet.gov.ar:11336/82620instacron: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 10:39:40.221CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Advances in the synthesis of 5-and 6-substituted uracil derivatives
title Advances in the synthesis of 5-and 6-substituted uracil derivatives
spellingShingle Advances in the synthesis of 5-and 6-substituted uracil derivatives
Bardagi, Javier Ivan
MINI REVIEW
SYNTHESIS
5- and 6- DERIVATES
URACIL
title_short Advances in the synthesis of 5-and 6-substituted uracil derivatives
title_full Advances in the synthesis of 5-and 6-substituted uracil derivatives
title_fullStr Advances in the synthesis of 5-and 6-substituted uracil derivatives
title_full_unstemmed Advances in the synthesis of 5-and 6-substituted uracil derivatives
title_sort Advances in the synthesis of 5-and 6-substituted uracil derivatives
dc.creator.none.fl_str_mv Bardagi, Javier Ivan
Rossi, Roberto Arturo
author Bardagi, Javier Ivan
author_facet Bardagi, Javier Ivan
Rossi, Roberto Arturo
author_role author
author2 Rossi, Roberto Arturo
author2_role author
dc.subject.none.fl_str_mv MINI REVIEW
SYNTHESIS
5- and 6- DERIVATES
URACIL
topic MINI REVIEW
SYNTHESIS
5- and 6- DERIVATES
URACIL
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The uracil unit is one of the most important structures in life, it being part of the building blocks of RNA and DNA and other natural products; therefore, it is not surprising that uracil derivatives have important biological activity. Uracil-based compounds are used in the treatment of cancer (5-fluoruracil) and against infections of the HIV virus (AZT). Actions as antiviral and antitumoral agents are perhaps the most widely reported activity. However, other uracil derivatives have been synthesized which are herbicides, insecticides, bactericides, acaricides, etc. In addition, uracil units can be found in the chemistry of peptide nucleic acid (PNA) or as part of other fused systems with antiallergic, antihypertensive, cardiotonic, bronchodilator or antibronchitis activity.The search for uracil derivatives has been carried out since the beginning of the last century and even today there is great interest in the development of new derivatives and strategies for synthesis so as to improve the yield of known compounds. To prepare uracils, there are three main synthetic strategies: a) building the uracil nucleus from acyclic precursors with appropriate substituents; b)modification of the structure of functionalized uracils or uracil itself by reaction with different reagents, as the recent synthesis of 5-trifluoromethyluracil and uridines with oxiranyl and tetrahydrofuranyl substituents; c) functionalization of masked uracil moieties with reactions incompatible with the nucleus, for example the synthesis of 6-aryl and 6- acyluracils and 2 -eoxypseudouridine. Combinations of these approaches are often found in the synthesis of target compounds with potential biological activities.The present review will cover advances in the synthesis of 5- and 6-substituted uracils over the last 8-10 years. This review has been organized in terms of the type of union that links the uracil moieties to the substitution groups; fused systems will have a separate section.
Fil: Bardagi, Javier Ivan. 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
description The uracil unit is one of the most important structures in life, it being part of the building blocks of RNA and DNA and other natural products; therefore, it is not surprising that uracil derivatives have important biological activity. Uracil-based compounds are used in the treatment of cancer (5-fluoruracil) and against infections of the HIV virus (AZT). Actions as antiviral and antitumoral agents are perhaps the most widely reported activity. However, other uracil derivatives have been synthesized which are herbicides, insecticides, bactericides, acaricides, etc. In addition, uracil units can be found in the chemistry of peptide nucleic acid (PNA) or as part of other fused systems with antiallergic, antihypertensive, cardiotonic, bronchodilator or antibronchitis activity.The search for uracil derivatives has been carried out since the beginning of the last century and even today there is great interest in the development of new derivatives and strategies for synthesis so as to improve the yield of known compounds. To prepare uracils, there are three main synthetic strategies: a) building the uracil nucleus from acyclic precursors with appropriate substituents; b)modification of the structure of functionalized uracils or uracil itself by reaction with different reagents, as the recent synthesis of 5-trifluoromethyluracil and uridines with oxiranyl and tetrahydrofuranyl substituents; c) functionalization of masked uracil moieties with reactions incompatible with the nucleus, for example the synthesis of 6-aryl and 6- acyluracils and 2 -eoxypseudouridine. Combinations of these approaches are often found in the synthesis of target compounds with potential biological activities.The present review will cover advances in the synthesis of 5- and 6-substituted uracils over the last 8-10 years. This review has been organized in terms of the type of union that links the uracil moieties to the substitution groups; fused systems will have a separate section.
publishDate 2009
dc.date.none.fl_str_mv 2009-01
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/11336/82620
Bardagi, Javier Ivan; Rossi, Roberto Arturo; Advances in the synthesis of 5-and 6-substituted uracil derivatives; Routledge Journals, Taylor & Francis Ltd; Organic Preparations and Procedures International; 41; 6; 1-2009; 479-514
0030-4948
1945-5453
CONICET Digital
CONICET
url http://hdl.handle.net/11336/82620
identifier_str_mv Bardagi, Javier Ivan; Rossi, Roberto Arturo; Advances in the synthesis of 5-and 6-substituted uracil derivatives; Routledge Journals, Taylor & Francis Ltd; Organic Preparations and Procedures International; 41; 6; 1-2009; 479-514
0030-4948
1945-5453
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://www.tandfonline.com/doi/abs/10.1080/00304940903378776
info:eu-repo/semantics/altIdentifier/doi/10.1080/00304940903378776
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 Routledge Journals, Taylor & Francis Ltd
publisher.none.fl_str_mv Routledge Journals, Taylor & Francis Ltd
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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