Efficient Synthesis of Highly Enantioenriched Delta(1)-Pyrrolines
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10773/18209 |
Resumo: | A general and efficient asymmetric synthesis of Δ1-pyrrolines by a one-pot nitro-reduction, cyclization, and dehydration of (R,E)-1,5- diphenyl-3-(nitromethyl)-5-pent-4-en-1-ones with iron and aqueous hydrochloric acid has been developed. The Δ1-pyrrolines were obtained with excellent enantioselectivities (up to 99%) and high yields (up to 83%). |
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Efficient Synthesis of Highly Enantioenriched Delta(1)-PyrrolinesPyrrolinesReductive cyclizationMichael additionSstereoselectivityA general and efficient asymmetric synthesis of Δ1-pyrrolines by a one-pot nitro-reduction, cyclization, and dehydration of (R,E)-1,5- diphenyl-3-(nitromethyl)-5-pent-4-en-1-ones with iron and aqueous hydrochloric acid has been developed. The Δ1-pyrrolines were obtained with excellent enantioselectivities (up to 99%) and high yields (up to 83%).Thieme Publishing2017-08-02T13:59:49Z2015-01-01T00:00:00Z2015info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/18209eng1437-209610.1055/s-0034-1380144Resende, Diana I. S. P.Guieu, SamuelOliva, Cristina G.Silva, Artur M. S.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T11:33:38Zoai:ria.ua.pt:10773/18209Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:52:40.505772Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Efficient Synthesis of Highly Enantioenriched Delta(1)-Pyrrolines |
title |
Efficient Synthesis of Highly Enantioenriched Delta(1)-Pyrrolines |
spellingShingle |
Efficient Synthesis of Highly Enantioenriched Delta(1)-Pyrrolines Resende, Diana I. S. P. Pyrrolines Reductive cyclization Michael addition Sstereoselectivity |
title_short |
Efficient Synthesis of Highly Enantioenriched Delta(1)-Pyrrolines |
title_full |
Efficient Synthesis of Highly Enantioenriched Delta(1)-Pyrrolines |
title_fullStr |
Efficient Synthesis of Highly Enantioenriched Delta(1)-Pyrrolines |
title_full_unstemmed |
Efficient Synthesis of Highly Enantioenriched Delta(1)-Pyrrolines |
title_sort |
Efficient Synthesis of Highly Enantioenriched Delta(1)-Pyrrolines |
author |
Resende, Diana I. S. P. |
author_facet |
Resende, Diana I. S. P. Guieu, Samuel Oliva, Cristina G. Silva, Artur M. S. |
author_role |
author |
author2 |
Guieu, Samuel Oliva, Cristina G. Silva, Artur M. S. |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Resende, Diana I. S. P. Guieu, Samuel Oliva, Cristina G. Silva, Artur M. S. |
dc.subject.por.fl_str_mv |
Pyrrolines Reductive cyclization Michael addition Sstereoselectivity |
topic |
Pyrrolines Reductive cyclization Michael addition Sstereoselectivity |
description |
A general and efficient asymmetric synthesis of Δ1-pyrrolines by a one-pot nitro-reduction, cyclization, and dehydration of (R,E)-1,5- diphenyl-3-(nitromethyl)-5-pent-4-en-1-ones with iron and aqueous hydrochloric acid has been developed. The Δ1-pyrrolines were obtained with excellent enantioselectivities (up to 99%) and high yields (up to 83%). |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-01-01T00:00:00Z 2015 2017-08-02T13:59:49Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10773/18209 |
url |
http://hdl.handle.net/10773/18209 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1437-2096 10.1055/s-0034-1380144 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Thieme Publishing |
publisher.none.fl_str_mv |
Thieme Publishing |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799137577313239040 |