Efficient synthesis of multifunctional furanoid C-glycoamino acid precursors

[1]  Lai-Xi Wang,et al.  Synthesis, conformation, and immunogenicity of monosaccharide-centered multivalent HIV-1 gp41 peptides containing the sequence of DP178. , 2004, Bioorganic & medicinal chemistry.

[2]  T. Hirao,et al.  Highly ordered structures of peptides by using molecular scaffolds. , 2004, Chemical Society reviews.

[3]  Pastora Borrachero,et al.  Fluorination of 2-hydroxy-hexopyranosides by DAST: Towards formyl C-glycofuranosides from equatorial-2-OH methyl hexopyranosides , 2004 .

[4]  M. Whittaker,et al.  Tetrahydrofuran-based amino acids as library scaffolds. , 2004, Journal of combinatorial chemistry.

[5]  S. Gellman,et al.  Two Helical Conformations from a Single Foldamer Backbone: “Split Personality” in Short α/β‐Peptides , 2004 .

[6]  F. Schweizer,et al.  Unusual Amino Acids Accessed Through Sugar-Amino Acid Hybrids and Incorporation into Biologically Active Peptides , 2003 .

[7]  M. Sansom,et al.  Bend ribbon-forming tetrahydrofuran amino acids. , 2003, Organic & biomolecular chemistry.

[8]  Lai-Xi Wang,et al.  Cholic acid as template for multivalent peptide assembly. , 2003, Organic & biomolecular chemistry.

[9]  A. Zanka.  A simple and highly practical oxidation of primary alcohols to acids mediated by 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO). , 2003, Chemical & pharmaceutical bulletin.

[10]  B. Jaun,et al.  The fourth helical secondary structure of β-peptides: The (P)-28-helix of a β-hexapeptide consisting of (2R,3S)-3-amino-2-hydroxy acid residues , 2003 .

[11]  Lai-Xi Wang,et al.  Carbohydrate-centered maleimide cluster as a new type of templates for multivalent peptide assembling. synthesis of multivalent HIV-1 gp41 peptides. , 2003, Bioorganic & medicinal chemistry.

[12]  J. Tam,et al.  A facile ligation approach to prepare three-helix bundles of HIV fusion-state protein mimetics. , 2002, Organic letters.

[13]  S. Gellman,et al.  Stereoselective synthesis of 3-substituted 2-aminocyclopentanecarboxylic acid derivatives and their incorporation into short 12-helical beta-peptides that fold in water. , 2002, Journal of the American Chemical Society.

[14]  P. Perlmutter,et al.  β-amino acids: Versatile peptidomimetics , 2002 .

[15]  Yi-An Lu,et al.  Antimicrobial dendrimeric peptides. , 2002, European journal of biochemistry.

[16]  H. Kessler,et al.  Carbohydrate-based mimetics in drug design: sugar amino acids and carbohydrate scaffolds. , 2002, Chemical reviews.

[17]  F. Schweizer.  Glycosamino acids: building blocks for combinatorial synthesis-implications for drug discovery. , 2002, Angewandte Chemie.

[18]  D. Seebach,et al.  Synthesis of cyclo-β-tripeptides and their biological in vitro evaluation as antiproliferatives against the growth of human cancer cell lines , 2001 .

[19]  P. Balaram,et al.  Design of folded peptides. , 2001, Chemical reviews.

[20]  J. Thiery,et al.  Design, synthesis and preliminary biological evaluation of a focused combinatorial library of stereodiverse carbohydrate-scaffold-based peptidomimetics. , 2001, Bioorganic & medicinal chemistry.

[21]  G. Mclendon,et al.  Disruption of protein-protein interactions: design of a synthetic receptor that blocks the binding of cytochrome c to cytochrome c peroxidase. , 2001, Chemical communications.

[22]  D. Coppola,et al.  Design of GFB-111, a platelet-derived growth factor binding molecule with antiangiogenic and anticancer activity against human tumors in mice , 2000, Nature Biotechnology.

[23]  Pastora Borrachero,et al.  Rearrangement reactions in the fluorination of 3-deoxy-3-C-methyl-3-nitro-hexopyranosides (and hexo-1-thiopyranosides) of the d- and l-series by the DAST reagent , 2000 .

[24]  S. Gellman,et al.  12-Helix Formation in Aqueous Solution with Short β-Peptides Containing Pyrrolidine-Based Residues , 2000 .

[25]  Martin D. Smith,et al.  Designing secondary structures: 5‐azidomethyl tetrahydrofuran‐2‐carboxylates as carbohydrate‐derived dipeptide isosteres , 1999, Journal of peptide science : an official publication of the European Peptide Society.

[26]  L. Pickering,et al.  3-Azidotetrahydrofuran-2-carboxylates: monomers for five-ring templated β-amino acid foldamers? , 1999 .

[27]  D. Hoyer,et al.  Synthesis and Biological Evaluation of a Cyclo-β-tetrapeptide as a Somatostatin Analogue. , 1999, Angewandte Chemie.

[28]  A. Hamilton,et al.  Protein Surface Recognition by Synthetic Receptors: A Route to Novel Submicromolar Inhibitors for α-Chymotrypsin , 1999 .

[29]  Douglas R. Powell,et al.  Residue-based control of helix shape in β-peptide oligomers , 1997, Nature.

[30]  F. Cabrera-Escribano,et al.  Novel rearrangement reactions in the fluorination of methyl 3-C-methyl-3-nitro-α-l-hexopyranosides by the DAST reagent , 1997 .

[31]  J. Tam,et al.  Recent advances in multiple antigen peptides. , 1996, Journal of immunological methods.

[32]  M. Mutter,et al.  Protein design as a challenge for peptide chemists , 1995, Journal of peptide science : an official publication of the European Peptide Society.

[33]  K. Nicolaou,et al.  Carbonucleotoids and carbopeptoids: New carbohydrate oligomers , 1995 .

[34]  M. Mutter,et al.  Chemoselective ligation of multifunctional peptides to topological templates via thioether formation for TASP synthesis , 1995 .

[35]  H. H. Baer,et al.  Synthesis of the methyl 3-amino-3-deoxy-α- and β-d-allopyranosides and -allofuranosides , 1991 .

[36]  H. H. Baer,et al.  A facile formation of 2,5-anhydro sugars by ring contraction in methyl hexopyranoside 2-triflates under conditions of nucleophilic displacement. , 1989, Carbohydrate research.