CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 1999, Vol. 71, No. 5, pp. 729-744

http://dx.doi.org/10.1351/pac199971050729

New aspects of glycoside bond formation

R. R. Schmidt, J. C. Castro-Palomino and O. Retz

CrossRef Cited-by theme picture

CrossRef Cited-by Linking

  • Kim Minkyu, Lim Eunyoung, Jung Mankil: First total synthesis of natural pulsatilla saponin D via highly stereospecific glycosylation. Tetrahedron 2013, 69, 5481. <http://dx.doi.org/10.1016/j.tet.2013.04.095>
  • Kuryanov V. O., Luschtshyk A. A., Chupakhina T. A.: Glycosylated derivatives of substituted hydroxylamine. II. The phase transfer synthesis and the study of the glycosyl transfer reaction of glucosaminides of substituted hydroxylamine. Russ J Bioorg Chem 2013, 39, 426. <http://dx.doi.org/10.1134/S1068162013030084>
  • Bini Davide, Gregori Maria, Cosentino Ugo, Moro Giorgio, Canales Angeles, Capitoli Alice, Jiménez-Barbero Jesús, Cipolla Laura: Synthesis and characterization of a paramagnetic sialic acid conjugate as probe for magnetic resonance applications. Carbohydrate Research 2012, 354, 21. <http://dx.doi.org/10.1016/j.carres.2012.03.002>
  • El Ashry El Sayed H., Aly Aly A., Amer Mohammed R., Shah Muhammad R., Ng Seik W.: Synthesis and X-ray analysis of butyl and glycosyl (2-arylamino-4,4-dimethyl-6-oxocyclohex-1-ene)carbodithioates and their possible cyclization to 2-thioxo-6,7-dihydro-1H-benzo[d][1,3]thiazin-5(2H)-one derivatives. Carbohydrates Research 2011, 346, 169. <http://dx.doi.org/10.1016/j.carres.2010.11.005>
  • Kajjout Mohammed, Rolando Christian: Regiospecific synthesis of quercetin O-β-d-glucosylated and O-β-d-glucuronidated isomers. Tetrahedron 2011, 67, 4731. <http://dx.doi.org/10.1016/j.tet.2011.03.110>
  • Lawandi Janice, Rocheleau Sylvain, Moitessier Nicolas: Directing/protecting groups mediate highly regioselective glycosylation of monoprotected acceptors. Tetrahed 2011, 67, 8411. <http://dx.doi.org/10.1016/j.tet.2011.07.026>
  • Schmidt Richard R., Castro-Palomino Julio C., Retz Oliver: ChemInform Abstract: New Aspects of Glycoside Bond Formation. ChemInform 2010, 30, no. <http://dx.doi.org/10.1002/chin.199952262>
  • Frąckowiak Anna, Skibiński Przemysław, Gaweł Wiesław, Zaczyńska Ewa, Czarny Anna, Gancarz Roman: Synthesis of glycoside derivatives of hydroxyanthraquinone with ability to dissolve and inhibit formation of crystals of calcium oxalate. Potential compounds in kidney stone therapy. Eur J Med Chem 2010, 45, 1001. <http://dx.doi.org/10.1016/j.ejmech.2009.11.042>
  • Zhu Jianglong, Wan Qian, Ragupathi Govind, George Constantine M., Livingston Philip O., Danishefsky Samuel J.: Biologics through Chemistry: Total Synthesis of a Proposed Dual-Acting Vaccine Targeting Ovarian Cancer by Orchestration of Oligosaccharide and Polypeptide Domains. J Am Chem Soc 2009, 131, 4151. <http://dx.doi.org/10.1021/ja810147j>
  • Zhu Jianglong, Wan Qian, Lee Dongjoo, Yang Guangbin, Spassova Maria K., Ouerfelli Ouathek, Ragupathi Govind, Damani Payal, Livingston Philip O., Danishefsky Samuel J.: From Synthesis to Biologics: Preclinical Data on a Chemistry Derived Anticancer Vaccine. J Am Chem Soc 2009, 131, 9298. <http://dx.doi.org/10.1021/ja901415s>
  • Lee Dongjoo, Krauss Isaac J., Danishefsky Samuel J., Jeon Insik: A New Model for the Presentation of Tumor-Associated Antigens and the Quest for an Anticancer Vaccine: A Solution to the Synthesis Challenge via Ring-Closing Metathesis. J Am Chem Soc 2009, 131, 14337. <http://dx.doi.org/10.1021/ja9052625>
  • De Meo Cristina, Priyadarshani Uvege: C-5 Modifications in N-acetyl-neuraminic acid: scope and limitations. Carbohydrates Research 2008, 343, 1540. <http://dx.doi.org/10.1016/j.carres.2008.04.007>
  • van den Bos Leendert J., Codée Jeroen D. C., Litjens Remy E. J. N., Dinkelaar Jasper, Overkleeft Herman S., van der Marel Gijsbert A.: Uronic Acids in Oligosaccharide Synthesis. Eur J Org Chem 2007, 2007, 3963. <http://dx.doi.org/10.1002/ejoc.200700101>
  • Tian Qiang, Zhu Xing‐Mei, Yang Jin‐Song: Amberlyst 15–Catalyzed Efficient Synthesis of 2,3‐Unsaturated Glycosides via Ferrier Rearrangement for Glycal. Synth Comm 2007, 37, 691. <http://dx.doi.org/10.1080/00397910601131353>
  • Coullerez Géraldine, Seeberger Peter H., Textor Marcus: Merging Organic and Polymer Chemistries to Create Glycomaterials for Glycomics Applications. Macromol Biosci 2006, 6, 634. <http://dx.doi.org/10.1002/mabi.200600090>
  • Röhrig Christoph H., Retz Oliver A., Hareng Lars, Hartung Thomas, Schmidt Richard R.: A New Strategy for the Synthesis of Dinucleotides Loaded with Glycosylated Amino Acids-Investigations on in vitro Non-natural Amino Acid Mutagenesis for Glycoprotein Synthesis. Chem Eur J of Chem Bio 2005, 6, 1805. <http://dx.doi.org/10.1002/cbic.200500079>
  • Werz Daniel B., Seeberger Peter H.: Carbohydrates as the Next Frontier in Pharmaceutical Research. Chem Eur J 2005, 11, 3194. <http://dx.doi.org/10.1002/chem.200500025>
  • Jayakanthan K., Vankar Yashwant D.: Glycosyl trichloroacetylcarbamate: a new glycosyl donor for O-glycosylation. Carbohydrates Research 2005, 340, 2688. <http://dx.doi.org/10.1016/j.carres.2005.07.024>
  • Seeberger Peter H., Werz Daniel B.: Automated synthesis of oligosaccharides as a basis for drug discovery. Nat Rev Drug Disc 2005, 4, 751. <http://dx.doi.org/10.1038/nrd1823>
  • Röhrig Christoph H., Retz Oliver A., Meergans Thomas, Schmidt Richard R.: In vitro non-natural amino acid mutagenesis using a suppressor tRNA generated by the cis-acting hepatitis delta virus ribozyme. BIOPHYS BIOCHEM RES COMMUN 2004, 325, 731. <http://dx.doi.org/10.1016/j.bbrc.2004.10.086>
  • Misra Anup Kumar, Agnihotri Geetanjali, Madhusudan Soni Kamlesh, Tiwari Pallavi: Practical Synthesis of Sulfated Analogs of Lactosamine and Sialylated Lactosamine Derivatives. J Carbohydr Chem 2004, 23, 191. <http://dx.doi.org/10.1081/CAR-200030027>
  • Davis Benjamin G.: Synthesis of Glycoproteins. Chem. Rev. 2002, 102, 579. <http://dx.doi.org/10.1021/cr0004310>
  • Hirooka Motoko, Terayama Megumi, Mitani Emi, Koto Shinkiti, Miura Asako, Chiba Kayo, Takabatake Ayano, Tashiro Takako: Synthesis of Methyl O-α-D-Mannosyl-(1→4)-[(3-O-methyl-α-D- mannosyl)-(1→4)-]n3-O-methyl-α-D-mannosides (n = 0, 1, and 2) via Dehydrative Glycosylation. Bull Chem Soc Jpn 2002, 75, 1301. <http://dx.doi.org/10.1246/bcsj.75.1301>
  • Speer Oliver, Leist Marcel, Schmidt Richard R., Castro-Palomino Julio C., Simon Bernadett: Synthesis of Ganglioside GD3 and its Comparison with Bovine GD3 with Regard to Oligodendrocyte Apoptosis Mitochondrial Damage. Chem Eur J 2001, 7, 2178. <http://dx.doi.org/10.1002/1521-3765(20010518)7:10<2178::AID-CHEM2178>3.0.CO;2-E>
  • Li Xiaoliu, Ohtake Hiro, Takahashi Hideyo, Ikegami Shiro: A facile synthesis of 1′-C-alkyl-α-disaccharides from 1-C-alkyl-hexopyranoses and methyl 1-C-methyl-hexopyranosides. Tetrahedron 2001, 57, 4297. <http://dx.doi.org/10.1016/S0040-4020(01)00321-0>
  • Duclos Richard I.: The total synthesis of ganglioside GM3. Carbohydrates Research 2000, 328, 489. <http://dx.doi.org/10.1016/S0008-6215(00)00121-X>