2-Benzothiazolyl 1-Thiofuranosides -Synthesis and Application

J.      Bogusiak

doi:10.2174/1570178053765311

Abstract

2-Benzothiazolyl 1-thiofuranosides derivatives of L-arabino-,D-ribo-and D-xylofuranose were synthesized in good yield in a one-pot reaction by treatment of reducing monosaccharides with diphenyl phosphorochloridate and 2-mercaptobenzothiazol under phase-transfer conditions.Their ability to act as glycosyl donors was demonstrated.

Keywords: thiosugars, glycosylation, glycofuranosyl donors, glycofuranosides

« Previous Next »

Rights & Permissions Print Cite

Letters in Organic Chemistry

Title: 2-Benzothiazolyl 1-Thiofuranosides -Synthesis and Application

Volume: 2 Issue: 3

Author(s): J. Bogusiak

Affiliation:

Keywords: thiosugars, glycosylation, glycofuranosyl donors, glycofuranosides

Abstract: 2-Benzothiazolyl 1-thiofuranosides derivatives of L-arabino-,D-ribo-and D-xylofuranose were synthesized in good yield in a one-pot reaction by treatment of reducing monosaccharides with diphenyl phosphorochloridate and 2-mercaptobenzothiazol under phase-transfer conditions.Their ability to act as glycosyl donors was demonstrated.

Export Options

Export File:

RIS (for EndNote, Reference Manager, ProCite)

BibTeX

Text

Content:

Citation Only

Citation and Abstract

About this article

Cite this article as:

Bogusiak J., 2-Benzothiazolyl 1-Thiofuranosides -Synthesis and Application, Letters in Organic Chemistry 2005; 2 (3) . https://dx.doi.org/10.2174/1570178053765311