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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/82620
Ver los metadatos del registro completo
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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/ |
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application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Routledge Journals, Taylor & Francis Ltd |
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Routledge Journals, Taylor & Francis Ltd |
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reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
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CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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