Mycothiol synthesis by an anomerization reaction through endocyclic cleavage

8Citations
Citations of this article
10Readers
Mendeley users who have this article in their library.

Abstract

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.

Cite

CITATION STYLE

APA

Manabe, S., & Ito, Y. (2016). Mycothiol synthesis by an anomerization reaction through endocyclic cleavage. Beilstein Journal of Organic Chemistry, 12, 328–333. https://doi.org/10.3762/bjoc.12.35

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free