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Mycothiol synthesis by an anomerization reaction through endocyclic cleavage

Mycothiol is found in Gram-positive bacteria, where it helps in maintaining a reducing intracellular environment and it plays an important role in protecting the cell from toxic chemicals. The inhibition of the mycothiol biosynthesis is considered as a treatment for tuberculosis. Mycothiol contains...

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Detalles Bibliográficos
Autores principales: Manabe, Shino, Ito, Yukishige
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778527/
https://www.ncbi.nlm.nih.gov/pubmed/26977192
http://dx.doi.org/10.3762/bjoc.12.35
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author Manabe, Shino
Ito, Yukishige
author_facet Manabe, Shino
Ito, Yukishige
author_sort Manabe, Shino
collection PubMed
description Mycothiol is found in Gram-positive bacteria, where it helps in maintaining a reducing intracellular environment and it plays an important role in protecting the cell from toxic chemicals. The inhibition of the mycothiol biosynthesis is considered as a treatment for tuberculosis. Mycothiol contains an α-aminoglycoside, which is difficult to prepare stereoselectively by a conventional glycosylation reaction. In this study, mycothiol was synthesized by an anomerization reaction from an easily prepared β-aminoglycoside through endocyclic cleavage.
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spelling pubmed-47785272016-03-14 Mycothiol synthesis by an anomerization reaction through endocyclic cleavage Manabe, Shino Ito, Yukishige Beilstein J Org Chem Letter Mycothiol is found in Gram-positive bacteria, where it helps in maintaining a reducing intracellular environment and it plays an important role in protecting the cell from toxic chemicals. The inhibition of the mycothiol biosynthesis is considered as a treatment for tuberculosis. Mycothiol contains an α-aminoglycoside, which is difficult to prepare stereoselectively by a conventional glycosylation reaction. In this study, mycothiol was synthesized by an anomerization reaction from an easily prepared β-aminoglycoside through endocyclic cleavage. Beilstein-Institut 2016-02-22 /pmc/articles/PMC4778527/ /pubmed/26977192 http://dx.doi.org/10.3762/bjoc.12.35 Text en Copyright © 2016, Manabe and Ito https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Manabe, Shino
Ito, Yukishige
Mycothiol synthesis by an anomerization reaction through endocyclic cleavage
title Mycothiol synthesis by an anomerization reaction through endocyclic cleavage
title_full Mycothiol synthesis by an anomerization reaction through endocyclic cleavage
title_fullStr Mycothiol synthesis by an anomerization reaction through endocyclic cleavage
title_full_unstemmed Mycothiol synthesis by an anomerization reaction through endocyclic cleavage
title_short Mycothiol synthesis by an anomerization reaction through endocyclic cleavage
title_sort mycothiol synthesis by an anomerization reaction through endocyclic cleavage
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778527/
https://www.ncbi.nlm.nih.gov/pubmed/26977192
http://dx.doi.org/10.3762/bjoc.12.35
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