期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2012, 期 23, 页码 4333-4338出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201200299
关键词
Thioethers; Glycosylation; Glycosides; Selenium; Synthetic methods
A series of 3-thioglycosylated 5,6-diacetoxyindole derivatives, which are important tools for eumelanin research and application, were prepared through a practical and efficient approach exploiting a dynamic mixture of thioglycoside agents. The strategy is feasible for installing both mono- and disaccharide units and relies on the facile in situ conversion of glycosyl disulfides into the corresponding, more reactive, phenylselenenyl sulfides in the presence of diphenyl diselenide, N-bromosuccinimide (NBS) and tetrabutylammonium bromide (TBAB).
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