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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2016
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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. |
format | Online Article Text |
id | pubmed-4778527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT manabeshino mycothiolsynthesisbyananomerizationreactionthroughendocycliccleavage AT itoyukishige mycothiolsynthesisbyananomerizationreactionthroughendocycliccleavage |