Title of article
Synthesis of rapamycin glycoconjugates via a CuAAC-based approach
Author/Authors
Moni، نويسنده , , Lisa and Marra، نويسنده , , Alberto and Skotnicki، نويسنده , , Jerauld S. and Koehn، نويسنده , , Frank E. and Abou-Gharbia، نويسنده , , Magid and Dondoni، نويسنده , , Alessandro، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2013
Pages
5
From page
6999
To page
7003
Abstract
The conversion of the C40 secondary hydroxyl group of rapamycin into the azido group was followed by copper catalyzed cycloaddition of the resulting azido-rapamcin with various unprotected propargyl O- and S-glycosides and a C-ethynyl derivative. This approach furnished a collection of triazole-bridged rapamycin glycoconjugates (14 examples) in 44–83% isolated yield.
Keywords
Azido-rapamycin , cycloaddition , Triazole , Sugar alkyne
Journal title
Tetrahedron Letters
Serial Year
2013
Journal title
Tetrahedron Letters
Record number
1886998
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