Synthesis of potential inhibitors of hemagglutination by influenza virus: chemoenzymic preparation of N-5 analogs of N-acetylneuraminic acid.

[1]  J. Fisher,et al.  Peptide to glycopeptide: glycosylated oligopeptide renin inhibitors with attenuated in vivo clearance properties. , 1991, Journal of medicinal chemistry.

[2]  J. Knowles,et al.  Monovalent sialosides that bind tightly to influenza A virus. , 1991, Journal of medicinal chemistry.

[3]  G. Whitesides,et al.  Synthesis of the α-methyl ketoside of 5-amino neuraminic acid methyl ester and its corresponding 5-myristoyl and 5-cyclopropanoyl derivative , 1990 .

[4]  R. Roy,et al.  Synthesis of protein conjugates and analogues of N-acetylneuraminic acid , 1990 .

[5]  G M Whitesides,et al.  Hemagglutinins from two influenza virus variants bind to sialic acid derivatives with millimolar dissociation constants: a 500-MHz proton nuclear magnetic resonance study. , 1989, Biochemistry.

[6]  J. Paulson,et al.  4-O-acetyl-N-acetylneuraminic acid in the N-linked carbohydrate structures of equine and guinea pig alpha 2-macroglobulins, potent inhibitors of influenza virus infection. , 1989, The Journal of biological chemistry.

[7]  K. Okamoto,et al.  Glycosidation of sialic acid , 1989 .

[8]  G. Air,et al.  The neuraminidase of influenza virus , 1989, Proteins.

[9]  S. Cusack,et al.  Structure of the influenza virus haemagglutinin complexed with its receptor, sialic acid , 1988, Nature.

[10]  S. Danishefsky,et al.  Stereoselective total syntheses of the naturally occurring enantiomers of N-acetylneuraminic acid and 3-deoxy-D-manno-2-octulosonic acid. A new and stereospecific approach to sialo and 3-deoxy-D-manno-2-octulosonic acid conjugates , 1988 .

[11]  W. Schmid,et al.  Structural variations of N‐acetylneuraminic acid, 9. A new useful approach to the epimers at C‐7 and C‐7,8 of N‐acetylneuraminic acid , 1988 .

[12]  G. Whitesides,et al.  Membrane-enclosed enzymic catalysis (MEEC): a useful, practical new method for the manipulation of enzymes in organic synthesis , 1987 .

[13]  J. Skehel,et al.  The structure and function of the hemagglutinin membrane glycoprotein of influenza virus. , 1987, Annual review of biochemistry.

[14]  H. Ogura,et al.  Syntheses of 2-O-glycosyl derivatives of N-acetyl-d-neuraminic acid , 1986 .

[15]  A. Vasella,et al.  4‐Methylumbelliferyl 5‐Acetamido‐3,4,5‐trideoxy‐α‐D‐manno‐2‐nonulopyranosidonic Acid: Synthesis and Resistance to Bacterial Sialidases , 1986 .

[16]  H. Waldmann,et al.  DIRECTED STEREOSELECTIVE SYNTHESIS OF ALPHA-N-ACETYL AND BETA-N-ACETYL NEURAMINIC ACID GALACTOSE DISACCHARIDES USING 2-CHLORO AND 2-FLUORO DERIVATIVES OF NEURAMINIC ACID ALLYL ESTER , 1985 .

[17]  J. E. Mellema,et al.  Characterization of three highly purified influenza virus strains by electron microscopy. , 1984, The Journal of general virology.

[18]  J. Paulson,et al.  Selection of influenza virus variants based on sialyloligosaccharide receptor specificity , 1984 .

[19]  J. Paulson,et al.  Differential sensitivity of human, avian, and equine influenza A viruses to a glycoprotein inhibitor of infection: selection of receptor specific variants. , 1983, Virology.

[20]  J. Vliegenthart,et al.  A facile preparation of alkyl α-glycosides of the methyl ester of N-acetyl-D-neuraminic acid , 1982 .

[21]  W. C. Still,et al.  Rapid chromatographic technique for preparative separations with moderate resolution , 1978 .

[22]  M. Perry,et al.  Stepwise synthesis of N-acetylneuraminic acid and N-acetyl[1-13C]neuraminic acid , 1978 .

[23]  E. Corey,et al.  A key intermediate for the synthesis of maytansine and related antitumor agents , 1978 .

[24]  Carbon-13 nuclear magnetic resonance spin-lattice relaxation in the N-acylneuraminic acids. Probes for internal dynamics and conformational analysis , 1977 .

[25]  H. Faillard,et al.  Untersuchungen zur enzymatischen Spezifität der Neuraminidase und N-Acyl-neuraminat-Lyase in bezug auf die N-Substitution , 1969 .

[26]  E. D. Kilbourne.  Future influenza vaccines and the use of genetic recombinants. , 1969, Bulletin of the World Health Organization.

[27]  J. Cornforth,et al.  Preparation of N-acetyl-neuraminic acid from N-acetyl-D-mannosamine. , 1960, Biochimica et biophysica acta.

[28]  J. Brug,et al.  Configuration of N-acetylneuraminic Acid , 1958, Nature.

[29]  L. Svennerholm,et al.  Sialic acids in blood serum. , 1958, Biochimica et biophysica acta.

[30]  G. Uhlenbruck,et al.  [Cleavage of N-glycolylneuraminic acid (P-sialic acid) from porcine submaxillary mucin by the receptor-destroying enzyme]. , 1957, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

[31]  P. Bóhm,et al.  [Isolation of methoxyneuraminic acid as a product of cleavage of blood proteins]. , 1955, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

[32]  E. Baumann.  Ueber eine einfache Methode der Darstellung von Benzoësäureäthern , 1886 .

[33]  C. Schotten.  Ueber die Oxydation des Piperidins , 1883 .