Richard R. Schmidt

Research interests

Publications

• Neue Prinzipien für die Bildung von glycosidischen Bindungen

  Angewandte Chemie · 2009 · 10.1002/ange.200802036

• New Principles for Glycoside‐Bond Formation

  Angewandte Chemie International Edition · 2009 · https://doi.org/10.1002/anie.200802036

• Commensal bacteria regulate Toll-like receptor 3–dependent inflammation after skin injury

  Nature Medicine · 2009 · https://doi.org/10.1038/nm.2062

• The length of lipids bound to human CD1d molecules modulates the affinity of NKT cell TCR and the threshold of NKT cell activation

  The Journal of Experimental Medicine · 2007 · 10.1084/jem.20062342

• Activation of TLR2 and TLR4 by Glycosylphosphatidylinositols Derived from Toxoplasma gondii

  The Journal of Immunology · 2007 · 10.4049/jimmunol.179.2.1129

• The crystal structure of human CD1d with and without α-galactosylceramide

  Nature Immunology · 2005 · 10.1038/ni1225

• Synthetic Routes to Thiooligosaccharides and Thioglycopeptides

  Chemical Reviews · 2005 · 10.1021/cr040660c

• NKT Cells Enhance CD4+ and CD8+ T Cell Responses to Soluble Antigen In Vivo through Direct Interaction with Dendritic Cells

  The Journal of Immunology · 2003 · 10.4049/jimmunol.171.10.5140

• Synthetic Lipoteichoic Acid from Staphylococcus aureus Is a Potent Stimulus of Cytokine Release

  The Journal of Experimental Medicine · 2002 · 10.1084/jem.20020322

• Structure of human CD1b with bound ligands at 2.3 Å, a maze for alkyl chains

  Nature Immunology · 2002 · 10.1038/ni821

• Intramolecular O-Glycoside Bond Formation

  Chemical Reviews · 2000 · 10.1021/cr990307k

• Sphingosine 1-Phosphate-induced Cell Rounding and Neurite Retraction Are Mediated by the G Protein-coupled Receptor H218

  Journal of Biological Chemistry · 1999 · 10.1074/jbc.274.8.4626

• Anomeric-Oxygen Activation for Glycoside Synthesis: The Trichloroacetimidate Method

  Advances in carbohydrate chemistry and biochemistry · 1994 · https://doi.org/10.1016/s0065-2318(08)60150-x

• Efficient sialylation with phosphite as leaving group

  Tetrahedron Letters · 1992 · 10.1016/s0040-4039(00)60022-9

• Glycosylation with highly reactive glycosyl donors: efficiency of the inverse procedure

  Tetrahedron Letters · 1991 · 10.1016/s0040-4039(00)92704-7

• Nitriles as Solvents in Glycosylation Reactions: Highly Selective β-Glycoside Synthesis 1

  Synlett · 1990 · 10.1055/s-1990-21214

• Sphingomyelin is synthesized in the cis Golgi

  FEBS Letters · 1990 · 10.1016/0014-5793(90)80659-7

• Neue Methoden zur Glycosid- und Oligosaccharidsynthese – gibt es Alternativen zur Koenigs-Knorr-Methode?

  Angewandte Chemie · 1986 · 10.1002/ange.19860980305

• New Methods for the Synthesis of Glycosides and Oligosaccharides—Are There Alternatives to the Koenigs‐Knorr Method? [New Synthetic Methods (56)]

  Angewandte Chemie International Edition in English · 1986 · https://doi.org/10.1002/anie.198602121

• Hetero-Diels-Alder reaction in highly functionalized natural product synthesis

  Accounts of Chemical Research · 1986 · 10.1021/ar00128a004

• Glycosylimidate, 12 Direkte Synthese von O‐α‐ und O‐β‐Glycosyl‐imidaten

  Liebigs Annalen der Chemie · 1984 · 10.1002/jlac.198419840710

• Glycosylimidate, 13. Anwendung des Trichloracetimidat‐Verfahrens auf 2‐Azidoglucose‐ und 2‐Azidogalactose‐Derivate

  Liebigs Annalen der Chemie · 1984 · 10.1002/jlac.198419841108

• Glycosylimidate, 8. Synthese von 1‐Thioglycosiden

  Liebigs Annalen der Chemie · 1983 · 10.1002/jlac.198319830717

• Einfache Synthese von α-und β-O-Glykosylimidaten; Herstellung von Glykosiden und Disacchariden

  Angewandte Chemie · 1980 · 10.1002/ange.19800920933

• Facile Synthesis of α‐ and β‐ O ‐Glycosyl Imidates; Preparation of Glycosides and Disaccharides

  Angewandte Chemie International Edition in English · 1980 · https://doi.org/10.1002/anie.198007311

Current projects

No projects listed.