The chemistry of isatins: a review from 1975 to 1999

Detalhes bibliográficos
Autor(a) principal: Silva,Joaquim F. M. da
Data de Publicação: 2001
Outros Autores: Garden,Simon J., Pinto,Angelo C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532001000300002
Resumo: Isatins (1H-indole-2,3-dione) are synthetically versatile substrates, where they can be used for the synthesis of a large variety of heterocyclic compounds, such as indoles and quinolines, and as raw material for drug synthesis. Isatins have also been found in mammalian tissue and their function as a modulator of biochemical processes has been the subject of several discussions. The advances in the use of isatins for organic synthesis during the last twenty-five years, as well as a survey of its biological and pharmacological properties are reported in this review and in the accompanying supplementary information.
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spelling The chemistry of isatins: a review from 1975 to 1999isatinheterocyclic synthesisdrug synthesismetal complexesIsatins (1H-indole-2,3-dione) are synthetically versatile substrates, where they can be used for the synthesis of a large variety of heterocyclic compounds, such as indoles and quinolines, and as raw material for drug synthesis. Isatins have also been found in mammalian tissue and their function as a modulator of biochemical processes has been the subject of several discussions. The advances in the use of isatins for organic synthesis during the last twenty-five years, as well as a survey of its biological and pharmacological properties are reported in this review and in the accompanying supplementary information.Sociedade Brasileira de Química2001-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532001000300002Journal of the Brazilian Chemical Society v.12 n.3 2001reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532001000300002info:eu-repo/semantics/openAccessSilva,Joaquim F. M. daGarden,Simon J.Pinto,Angelo C.eng2001-10-02T00:00:00Zoai:scielo:S0103-50532001000300002Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2001-10-02T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv The chemistry of isatins: a review from 1975 to 1999
title The chemistry of isatins: a review from 1975 to 1999
spellingShingle The chemistry of isatins: a review from 1975 to 1999
Silva,Joaquim F. M. da
isatin
heterocyclic synthesis
drug synthesis
metal complexes
title_short The chemistry of isatins: a review from 1975 to 1999
title_full The chemistry of isatins: a review from 1975 to 1999
title_fullStr The chemistry of isatins: a review from 1975 to 1999
title_full_unstemmed The chemistry of isatins: a review from 1975 to 1999
title_sort The chemistry of isatins: a review from 1975 to 1999
author Silva,Joaquim F. M. da
author_facet Silva,Joaquim F. M. da
Garden,Simon J.
Pinto,Angelo C.
author_role author
author2 Garden,Simon J.
Pinto,Angelo C.
author2_role author
author
dc.contributor.author.fl_str_mv Silva,Joaquim F. M. da
Garden,Simon J.
Pinto,Angelo C.
dc.subject.por.fl_str_mv isatin
heterocyclic synthesis
drug synthesis
metal complexes
topic isatin
heterocyclic synthesis
drug synthesis
metal complexes
description Isatins (1H-indole-2,3-dione) are synthetically versatile substrates, where they can be used for the synthesis of a large variety of heterocyclic compounds, such as indoles and quinolines, and as raw material for drug synthesis. Isatins have also been found in mammalian tissue and their function as a modulator of biochemical processes has been the subject of several discussions. The advances in the use of isatins for organic synthesis during the last twenty-five years, as well as a survey of its biological and pharmacological properties are reported in this review and in the accompanying supplementary information.
publishDate 2001
dc.date.none.fl_str_mv 2001-06-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532001000300002
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532001000300002
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532001000300002
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.12 n.3 2001
reponame:Journal of the Brazilian Chemical Society (Online)
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reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
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