Hexafluoroacetone as a Protecting and Activating Reagent. <Emphasis Type="Italic">N</Emphasis>- and <Emphasis Type="Italic">O</Emphasis>-Glycosylation of Isoserine and Isocysteine期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Hexafluoroacetone as a Protecting and Activating Reagent. N- and O-Glycosylation of Isoserine and Isocysteine

Authors:	Christoph?B?ttcher,Jan?Spengler,Lothar?Hennig,Fernando?Albericio,Klaus?Burger author-information" > author-information__contact u-icon-before" > mailto:burger@organik.chemie.uni-leipzig.de" title=" burger@organik.chemie.uni-leipzig.de" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author

Affiliation:	(1) Department of Organic Chemistry, University of Leipzig, D-04103 Leipzig, Germany;(2) Institut de Recerca Biomèdica de Barcelona, Parc Cientific Barcelona, 08028 Barcelona, Spain

Abstract:	Summary. Starting from HFA-protected malic and thiomalic acid a series of O- and N-glycoconjugates suitable for peptide and depsipeptide modification has been synthesized.

Keywords:	. Malic acid Thiomalic acid Hexafluoroacetone Isocyanates Glycosylamines Glycoconjugates.
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