Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide

Detalhes bibliográficos
Autor(a) principal: Enugala, Ramu
Data de Publicação: 2012
Outros Autores: Marques, M. Manuel B.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/92206
Resumo: A simple and alternative route to a versatile N-acetyl glucosamine disaccharide building block was developed, possessing a free 3-hydroxyl group. In this strategy, the 2,2,2-trichloro-ethoxy carbonyl (Troc) group was used as an amino-and 3-hydroxyl-protecting group.
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spelling Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharideGlucosamineGlycosylationN-acetyl glucosamineTrichloro-ethoxycarbonyl groupOrganic ChemistryA simple and alternative route to a versatile N-acetyl glucosamine disaccharide building block was developed, possessing a free 3-hydroxyl group. In this strategy, the 2,2,2-trichloro-ethoxy carbonyl (Troc) group was used as an amino-and 3-hydroxyl-protecting group.CQFB-REQUIMTE - Centro de Química Fina e Biotecnologia (Lab. Associado REQUIMTE)DQ - Departamento de QuímicaRUNEnugala, RamuMarques, M. Manuel B.2020-02-04T23:35:47Z2012-02-052012-02-05T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article11application/pdfhttp://hdl.handle.net/10362/92206eng1551-7012PURE: 12929212https://doi.org/10.3998/ark.5550190.0013.608info: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:RCAAP2024-03-11T04:41:02Zoai:run.unl.pt:10362/92206Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:37:28.374411Repositório 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 Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide
title Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide
spellingShingle Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide
Enugala, Ramu
Glucosamine
Glycosylation
N-acetyl glucosamine
Trichloro-ethoxycarbonyl group
Organic Chemistry
title_short Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide
title_full Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide
title_fullStr Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide
title_full_unstemmed Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide
title_sort Synthesis of a 3-hydroxyl-free N-acetyl glucosamine disaccharide
author Enugala, Ramu
author_facet Enugala, Ramu
Marques, M. Manuel B.
author_role author
author2 Marques, M. Manuel B.
author2_role author
dc.contributor.none.fl_str_mv CQFB-REQUIMTE - Centro de Química Fina e Biotecnologia (Lab. Associado REQUIMTE)
DQ - Departamento de Química
RUN
dc.contributor.author.fl_str_mv Enugala, Ramu
Marques, M. Manuel B.
dc.subject.por.fl_str_mv Glucosamine
Glycosylation
N-acetyl glucosamine
Trichloro-ethoxycarbonyl group
Organic Chemistry
topic Glucosamine
Glycosylation
N-acetyl glucosamine
Trichloro-ethoxycarbonyl group
Organic Chemistry
description A simple and alternative route to a versatile N-acetyl glucosamine disaccharide building block was developed, possessing a free 3-hydroxyl group. In this strategy, the 2,2,2-trichloro-ethoxy carbonyl (Troc) group was used as an amino-and 3-hydroxyl-protecting group.
publishDate 2012
dc.date.none.fl_str_mv 2012-02-05
2012-02-05T00:00:00Z
2020-02-04T23:35:47Z
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10362/92206
url http://hdl.handle.net/10362/92206
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1551-7012
PURE: 12929212
https://doi.org/10.3998/ark.5550190.0013.608
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eu_rights_str_mv openAccess
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