@ARTICLE{Ibatullin20037961,
author={Ibatullin, F.M. and Shabalin, K.A. and Jänis, J.V. and Shavva, A.G.},
title={Reaction of 1,2-trans-glycosyl acetates with thiourea: A new entry to 1-thiosugars},
journal={Tetrahedron Letters},
year={2003},
volume={44},
number={43},
pages={7961-7964},
doi={10.1016/j.tetlet.2003.08.120},
note={cited By 63},
url={https://www.scopus.com/inward/record.uri?eid=2-s2.0-0141485298&doi=10.1016%2fj.tetlet.2003.08.120&partnerID=40&md5=9f2d0d8eeca517c0fc439d6beec3b1df},
affiliation={Molec./Radiation Biophysics Division, Petersburg Nuclear Physics Institute, Gatchina 188300, Russian Federation; Department of Chemistry, University of Joensuu, Joensuu, Finland; Chemical Department, Petersburg State University, St.-Petersburg, Russian Federation},
abstract={The reaction of 1,2-trans-glycosyl acetates with thiourea under boron trifluoride etherate catalysis affording acetylated S-glycosyl isothiourea derivatives is described. The isothiourea derivatives obtained can be readily transformed into the desired 1-thiosugar derivative by reaction with triethylamine and subsequent alkylation or acylation of the in situ formed 1-thioaldose. © 2003 Elsevier Ltd. All rights reserved.},
correspondence_address1={Ibatullin, F.M.; Molec./Radiation Biophysics Division, Petersburg Nuclear Physics Institute, Gatchina 188300, Russian Federation},
publisher={Elsevier Ltd},
issn={00404039},
coden={TELEA},
language={English},
abbrev_source_title={Tetrahedron Lett.},
document_type={Article},
source={Scopus},
}

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