[4+2] Cycloadditions between "in situ" generated α,α'-dioxothiones and unprotected or variously protected glycals provide a powerful synthetic way to obtain glycomimetics chemo-, regio- and stereoselectively. Examples of glycopeptidomimetics and mimetic of tumor antigens are reported.
Diels-Alder Based Synthesis of Glycomimetics / C. Nativi; E. Dragoni; B. Richichi; S. Roelens. - ELETTRONICO. - (2011), pp. 240-254. [10.2174/978160805277611101010240]
Diels-Alder Based Synthesis of Glycomimetics
NATIVI, CRISTINA;DRAGONI, ELISA;RICHICHI, BARBARA;
2011
Abstract
[4+2] Cycloadditions between "in situ" generated α,α'-dioxothiones and unprotected or variously protected glycals provide a powerful synthetic way to obtain glycomimetics chemo-, regio- and stereoselectively. Examples of glycopeptidomimetics and mimetic of tumor antigens are reported.File in questo prodotto:
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