Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II
Autor(a) principal: | |
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Data de Publicação: | 1997 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Química Nova (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40421997000100006 |
Resumo: | The hydroformylation reaction represents one of the most important C1-chemistry area in the chemical industry. This catalytic process, which has been developed up to now mainly to the production of commodities chemicals, has shown a remarkable potential for the preparation of several categories of specialty chemicals and in particular pharmaceutical compounds. Arylpropanoic acids, various amines containing aryl groups, and intermediates for the preparation of vitamins, carbocyclic and heterocyclic compounds and many other classes of organic molecules endowed with pharmacological activity are currently accessible in good-to-high yields through hydroformylation of selected olefinic substrates. The asymmetric hydroformylation is going to reach the stage of maturity and hence to contribute in solving many troublesome synthetic problems connected with the preparation of pharmacologically active compounds with very high enantiomeric purity. The present survey emphasizes the usefulness of synthesis gas as a starting material in fine chemistry, which is expected to be important for industry. |
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Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte IIhydroformylationaldehydesoptically active drugsThe hydroformylation reaction represents one of the most important C1-chemistry area in the chemical industry. This catalytic process, which has been developed up to now mainly to the production of commodities chemicals, has shown a remarkable potential for the preparation of several categories of specialty chemicals and in particular pharmaceutical compounds. Arylpropanoic acids, various amines containing aryl groups, and intermediates for the preparation of vitamins, carbocyclic and heterocyclic compounds and many other classes of organic molecules endowed with pharmacological activity are currently accessible in good-to-high yields through hydroformylation of selected olefinic substrates. The asymmetric hydroformylation is going to reach the stage of maturity and hence to contribute in solving many troublesome synthetic problems connected with the preparation of pharmacologically active compounds with very high enantiomeric purity. The present survey emphasizes the usefulness of synthesis gas as a starting material in fine chemistry, which is expected to be important for industry.Sociedade Brasileira de Química1997-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40421997000100006Química Nova v.20 n.1 1997reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0100-40421997000100006info:eu-repo/semantics/openAccessBotteghi,CarloMarchetti,MauroDel Ponte,Ginopor2008-09-24T00:00:00Zoai:scielo:S0100-40421997000100006Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2008-09-24T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II |
title |
Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II |
spellingShingle |
Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II Botteghi,Carlo hydroformylation aldehydes optically active drugs |
title_short |
Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II |
title_full |
Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II |
title_fullStr |
Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II |
title_full_unstemmed |
Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II |
title_sort |
Contribuições recentes da reação de hidroformilação na síntese de produtos farmacêuticos: parte II |
author |
Botteghi,Carlo |
author_facet |
Botteghi,Carlo Marchetti,Mauro Del Ponte,Gino |
author_role |
author |
author2 |
Marchetti,Mauro Del Ponte,Gino |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
Botteghi,Carlo Marchetti,Mauro Del Ponte,Gino |
dc.subject.por.fl_str_mv |
hydroformylation aldehydes optically active drugs |
topic |
hydroformylation aldehydes optically active drugs |
description |
The hydroformylation reaction represents one of the most important C1-chemistry area in the chemical industry. This catalytic process, which has been developed up to now mainly to the production of commodities chemicals, has shown a remarkable potential for the preparation of several categories of specialty chemicals and in particular pharmaceutical compounds. Arylpropanoic acids, various amines containing aryl groups, and intermediates for the preparation of vitamins, carbocyclic and heterocyclic compounds and many other classes of organic molecules endowed with pharmacological activity are currently accessible in good-to-high yields through hydroformylation of selected olefinic substrates. The asymmetric hydroformylation is going to reach the stage of maturity and hence to contribute in solving many troublesome synthetic problems connected with the preparation of pharmacologically active compounds with very high enantiomeric purity. The present survey emphasizes the usefulness of synthesis gas as a starting material in fine chemistry, which is expected to be important for industry. |
publishDate |
1997 |
dc.date.none.fl_str_mv |
1997-02-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40421997000100006 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40421997000100006 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
10.1590/S0100-40421997000100006 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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 |
Química Nova v.20 n.1 1997 reponame:Química Nova (Online) instname:Sociedade Brasileira de Química (SBQ) instacron:SBQ |
instname_str |
Sociedade Brasileira de Química (SBQ) |
instacron_str |
SBQ |
institution |
SBQ |
reponame_str |
Química Nova (Online) |
collection |
Química Nova (Online) |
repository.name.fl_str_mv |
Química Nova (Online) - Sociedade Brasileira de Química (SBQ) |
repository.mail.fl_str_mv |
quimicanova@sbq.org.br |
_version_ |
1750318100031471617 |