Towards the synthesis of aryl glucuronides as potential heparanase probes. An interesting outcome in the glycosidation of glucuronic acid with 4-hydroxycinnamic acid.

[1]  S. Iyer,et al.  Design and synthesis of dimeric heparinoid mimetics. , 2004, The Journal of organic chemistry.

[2]  R. Parekh,et al.  Biochemical characterization of the active heterodimer form of human heparanase (Hpa1) protein expressed in insect cells. , 2003, The Biochemical journal.

[3]  M. Nakajima,et al.  Structural Recognition by Recombinant Human Heparanase That Plays Critical Roles in Tumor Metastasis , 2002, The Journal of Biological Chemistry.

[4]  J. Elguero,et al.  A 13 C NMR study of the structure of four cinnamic acids and their methyl esters , 2001 .

[5]  I. Vlodavsky,et al.  Molecular properties and involvement of heparanase in cancer metastasis and angiogenesis. , 2001, The Journal of clinical investigation.

[6]  M. Yokoyama.  Methods of synthesis of glycosyl fluorides. , 2000, Carbohydrate research.

[7]  H. Nakano,et al.  Hydrolysis of β-glucosyl ester linkage of p-hydroxybenzoyl β-d-glucose, a chemically synthesized glucoside, by β-glucosidases , 2000 .

[8]  T. Kondo,et al.  Highly Efficient β-Glucosylation of the Acidic Hydroxyl Groups, Phenol and Carboxylic Acid, with an Peracetylated Glucosyl Fluoride Using a Combination of BF3 · Et2O and DTBMP as a Promoter , 1999 .

[9]  A. Marra,et al.  Design and Use of an Oxazolidine Silyl Enol Ether as a New Homoalanine Carbanion Equivalent for the Synthesis of Carbon-Linked Isosteres of O-Glycosyl Serine and N-Glycosyl Asparagine. , 1999, The Journal of organic chemistry.

[10]  A. Dinkova-Kostova,et al.  Chemoprotective properties of phenylpropenoids, bis(benzylidene)cycloalkanones, and related Michael reaction acceptors: correlation of potencies as phase 2 enzyme inducers and radical scavengers. , 1998, Journal of medicinal chemistry.

[11]  I. Vlodavsky,et al.  Substrate Specificity of Heparanases from Human Hepatoma and Platelets* , 1998, The Journal of Biological Chemistry.

[12]  A. Stachulski,et al.  The synthesis of O-glucuronides. , 1998, Natural product reports.

[13]  C. Monneret,et al.  p-NITROPHENYL -D-GLUCOPYRANOSIDURONIC ANALOGS AS POTENTIAL SUBSTRATES FOR -GLUCURONIDASE , 1997 .

[14]  A. Stachulski,et al.  Intermediates for Glucuronide Synthesis: 7-Hydroxycoumarin Glucuronide , 1997 .

[15]  V. Timoshchuk.  Uronic acids: synthesis and reactions , 1995 .

[16]  B. M. Pinto,et al.  Synthesis of a thio analogue of n-propyl kojibioside, a potential glucosidase inhibitor * , 1995 .

[17]  Chi‐Huey Wong,et al.  Synthesis and Use of Glycosyl Phosphites: An Effective Route to Glycosyl Phosphates, Sugar Nucleotides, and Glycosides , 1993 .

[18]  R. Miethchen,et al.  Reactions with and in anhydrous hydrogen fluoride systems. Part 8. Triethylamine trishydrofluoride — a convenient reagent for the stereoselective synthesis of glycosyl fluorides , 1993 .

[19]  R. Helm,et al.  Synthesis of feruloylated and p-coumaroylated methyl glycosides , 1992 .

[20]  L. Kjellén,et al.  Proteoglycans: structures and interactions. , 1991, Annual review of biochemistry.

[21]  J. Jacquinet.  Syntheses of the methyl glycosides of the repeating units of chondroitin 4- and 6-sulfate. , 1990, Carbohydrate research.

[22]  T. Tsuchiya.  Chemistry and developments of fluorinated carbohydrates. , 1990, Advances in carbohydrate chemistry and biochemistry.

[23]  B. Ernst,et al.  Preparation of glycosyl halides under neutral conditions , 1989 .

[24]  L. Tietze,et al.  Stereoselective synthesis of 1-O-trimethylsilyl-α- and -β-d-glucopyranuronate , 1986 .

[25]  R. R. Schmidt,et al.  O‐Glycosylimidate, 19. Reaktionen von Glycosyl‐trichloracetimidaten mit silylierten C‐Nucleophilen , 1985 .

[26]  P. Lartey,et al.  A new method for the synthesis of glycosyl fluorides , 1985 .

[27]  H. Kunz,et al.  Stereoselective glycosylation of Alcohols and Silyl Ethers Using Glycosyl Fluorides and Boron Trifluoride Etherate , 1985 .

[28]  G. Posner,et al.  A convenient, one-step, high-yield replacement of an anomeric hydroxyl group by a fluorine atom using dast. Preparation of glycosyl fluorides. , 1985 .

[29]  E. Keinan,et al.  A novel method for stereoselective glucuronidation , 1984 .

[30]  M. Hayashi,et al.  Glycosylation using glucopyranosyl fluorides and silicon-based catalysts. Solvent dependency of the stereoselection , 1984 .

[31]  K. Nicolaou,et al.  Practical synthesis of oligosaccharides. Partial synthesis of avermectin B1a , 1984 .

[32]  S. Shoda,et al.  STEREOSELECTIVE SYNTHESIS OF 1,2-CIS-GLYCOFURANOSIDES USING GLYCOFURANOSYL FLUORIDES , 1983 .

[33]  G. Snatzke,et al.  Über eine verbesserte Synthese von β-Glucosiduronsäure-Derivaten , 1983 .

[34]  K. Ham,et al.  N-hydroxyacetaminophen: a postulated toxic metabolite of acetaminophen. , 1981, Journal of medicinal chemistry.

[35]  S. Shoda,et al.  AN EFFICIENT METHOD FOR GLUCOSYLATION OF HYDROXY COMPOUNDS USING GLUCOPYRANOSYL FLUORIDE , 1981 .

[36]  R. Schmidt,et al.  Stereoselective glycosidations of uronic acids , 1980 .

[37]  A. Veyrières,et al.  Synthesis of 4-methylumbelliferyl 1,2-cis-glycosides☆ , 1978 .

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

[39]  Keitaro Kato,et al.  Synthesisof p-Nitrophenyl β-D-Glucopyranosiduronic Acid and Its Utilization as a Substrate for the Assay of β-Glucuronidase Activity , 1960 .

[40]  R. S. Murphey,et al.  Notes - A Synthesis ofo-Carboxyphenyl β-D-Glucopyranosiduronic Acid , 1956 .

[41]  J. W. Long,et al.  The Synthesis of Aryl-D-glucopyranosiduronic Acids1 , 1955 .