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Pure Appl. Chem., 1979, Vol. 51, No. 6, pp. 1219-1233

http://dx.doi.org/10.1351/pac197951061219

New methods in peptide synthesis, based on supernucleophiles

H. Eckert, W. Breuer, J. Geller, I. Lagerlund, M. Listl, D. Marquarding, S. Stuber, I. Ugi, S. Zahr and H. V. Zychlinski

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  • Ugi Ivar: Von Isocyaniden via Vierkomponenten-Kondensation zu Antibiotica-Synthesen. Angew Chem 2006, 94, 826. <http://dx.doi.org/10.1002/ange.19820941103>
  • Hayakawa Yoshihiro, Kawai Rie, Kataoka Masanori: Nucleotide synthesis via methods without nucleoside-base protection. Eur J Pharmaceutical Sci 2001, 13, 5. <http://dx.doi.org/10.1016/S0928-0987(00)00202-5>
  • Klösel Roland, König Stephan, Lehnhoff Stefan, Karl Rosa Maria: The 1,1- dianisyl-2,2,2-trichloroethyl group as 2′-hydroxyl protection of ribonucleotides. Tetrahedron 1996, 52, 1493. <http://dx.doi.org/10.1016/0040-4020(95)00981-7>
  • Karl Rosa Maria, Klösel Roland, König Stephan, Lehnhoff Stefan, Ugi Ivar: 1,1-Dianisyl-2,2,2-trichloroethyl ethers — A new protection for the hydroxyl group. Tetrahedron 1995, 51, 3759. <http://dx.doi.org/10.1016/0040-4020(95)00120-W>
  • Beaucage Serge L., Iyer Radhakrishman P.: Advances in the Synthesis of Oligonucleotides by the Phosphoramidite Approach. Tetrahedron 1992, 48, 2223. <http://dx.doi.org/10.1016/S0040-4020(01)88752-4>
  • Ugi Ivar, Bachmeier Norbert, Herrman Rudolpf, Jacob Peter, Karl Rosmarie, Klein Manuela, Landgraf Bernd, Lemmen Peter, Richter Wolfgang, Verfürth Uwe: Synthesis and Reactivity of Five-Membered Cyclic Phosphorylating Reagents and Other Auxiliaries for the Synthesis of Oligonucleotides. Phosphorus Sulfur Silicon Relat Elem 1990, 51, 57. <http://dx.doi.org/10.1080/10426509008040681>
  • Schneiderwind Ruth G.K., Ugi Ivar: Die 2,2,2-trichlor-t-butyloxycarbonyl-gruppe, eine neue n-schutzgruppe für oligonucleotidsynthesen. Tetrahedron 1983, 39, 2207. <http://dx.doi.org/10.1016/S0040-4020(01)91939-8>
  • Ugi Ivar: From Isocyanidesvia Four-Component Condensations to Antibiotic Syntheses. Angew Chem Int Ed Engl 1982, 21, 810. <http://dx.doi.org/10.1002/anie.198208101>
  • Kellner Herbert A., Schneiderwind Ruth G. K., Eckert Heiner, Ugi Ivar K.: Bis(2,2,2-trichlor-1,1-dimethylethyl)monochloro-phosphat, ein selektives Reagens für Phosphorylierung und Schutz der 5′-OH-Gruppe von Nucleosid-Derivaten. Angew Chem 1981, 93, 581. <http://dx.doi.org/10.1002/ange.19810930614>
  • Meggendorfer G., Schwarz R., Ugi I.: Darstellung von 2-(β-chloräthoxi)-2-oxo-4,5-dimethyl-1,3,2λ5-di-oxaphospholen, einem neuen phosphorylierungsmittel. Tetrahetron Lett 1980, 21, 2493. <http://dx.doi.org/10.1016/0040-4039(80)80109-2>