Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.

Detalhes bibliográficos
Autor(a) principal: Melo, Teresa M. V. D. Pinho e
Data de Publicação: 2006
Outros Autores: Lopes, Susana M. M., Gonsalves, Antonio M. d'A Rocha, Kaczor, Agnieszka, Fausto, Rui, Paixão, José A., Beja, Ana Matos, Silva, Manuela Ramos
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/17937
https://doi.org/10.2174/157017806779116996.
Resumo: A simple and efficient approach to the synthesis of the new chiral hexahydropyrrolo [1',2',5':3,4,5]thiazolo[3,4-c]oxazol-1-one ring system is reported. Infrared spectroscopy, quantum-chemical calculations and X-ray analysis allowed the stereochemistry assignment of (2aS,4aR,6aR)-2a,3,4,4a,6,6ahexahydropyrrolo-[ 1',2',5':3,4,5]thiazolo[3,4-c]oxazol-1-one. [ABSTRACT FROM AUTHOR]. Copyright of Letters in Organic Chemistry is the property of Bentham Science Publishers Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.).
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spelling Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.A simple and efficient approach to the synthesis of the new chiral hexahydropyrrolo [1',2',5':3,4,5]thiazolo[3,4-c]oxazol-1-one ring system is reported. Infrared spectroscopy, quantum-chemical calculations and X-ray analysis allowed the stereochemistry assignment of (2aS,4aR,6aR)-2a,3,4,4a,6,6ahexahydropyrrolo-[ 1',2',5':3,4,5]thiazolo[3,4-c]oxazol-1-one. [ABSTRACT FROM AUTHOR]. Copyright of Letters in Organic Chemistry is the property of Bentham Science Publishers Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.).Bentham Science2006-11info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/17937TID:15701786.http://hdl.handle.net/10316/17937https://doi.org/10.2174/157017806779116996.engMelo, Teresa M. V. D. Pinho eLopes, Susana M. M.Gonsalves, Antonio M. d'A RochaKaczor, AgnieszkaFausto, RuiPaixão, José A.Beja, Ana MatosSilva, Manuela Ramosinfo: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:RCAAP2021-10-07T09:43:27Zoai:estudogeral.uc.pt:10316/17937Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:01:45.479635Repositório 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 Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.
title Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.
spellingShingle Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.
Melo, Teresa M. V. D. Pinho e
title_short Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.
title_full Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.
title_fullStr Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.
title_full_unstemmed Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.
title_sort Hexahydro-Pyrrolo[1',2',5':3,4,5]Thiazolo[3,4-c]Oxazol-1-ones: New Chiral Tricyclic L-Cysteine and D-Penicillamine Derivatives.
author Melo, Teresa M. V. D. Pinho e
author_facet Melo, Teresa M. V. D. Pinho e
Lopes, Susana M. M.
Gonsalves, Antonio M. d'A Rocha
Kaczor, Agnieszka
Fausto, Rui
Paixão, José A.
Beja, Ana Matos
Silva, Manuela Ramos
author_role author
author2 Lopes, Susana M. M.
Gonsalves, Antonio M. d'A Rocha
Kaczor, Agnieszka
Fausto, Rui
Paixão, José A.
Beja, Ana Matos
Silva, Manuela Ramos
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Melo, Teresa M. V. D. Pinho e
Lopes, Susana M. M.
Gonsalves, Antonio M. d'A Rocha
Kaczor, Agnieszka
Fausto, Rui
Paixão, José A.
Beja, Ana Matos
Silva, Manuela Ramos
description A simple and efficient approach to the synthesis of the new chiral hexahydropyrrolo [1',2',5':3,4,5]thiazolo[3,4-c]oxazol-1-one ring system is reported. Infrared spectroscopy, quantum-chemical calculations and X-ray analysis allowed the stereochemistry assignment of (2aS,4aR,6aR)-2a,3,4,4a,6,6ahexahydropyrrolo-[ 1',2',5':3,4,5]thiazolo[3,4-c]oxazol-1-one. [ABSTRACT FROM AUTHOR]. Copyright of Letters in Organic Chemistry is the property of Bentham Science Publishers Ltd. and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.).
publishDate 2006
dc.date.none.fl_str_mv 2006-11
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/17937
TID:15701786.
http://hdl.handle.net/10316/17937
https://doi.org/10.2174/157017806779116996.
url http://hdl.handle.net/10316/17937
https://doi.org/10.2174/157017806779116996.
identifier_str_mv TID:15701786.
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