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Pure Appl. Chem., 1982, Vol. 54, No. 12, pp. 2537-2544

http://dx.doi.org/10.1351/pac198254122537

Studies on the total synthesis of streptogramin antibiotics: griseoviridin and madumycin (A-2315A)

A. I. Meyers, Jon Lawson, R. A. Amos, D. G. Walker and R. F. Spohn

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  • Liu Le, Xu Shimin, Zhou Hongwei: Silver carboxylate promoted lactonization: a general method applicable to prepare medium and large-sized lactones without high dilution or slow addition. Tetrahedron 2013, 69, 8386. <http://dx.doi.org/10.1016/j.tet.2013.07.064>
  • Braun Manfred, Mahler Hellmut: Non-chelate-controlled addition of 1-Bromo-1-lithio-1-alkenes toO-protected lactaldehydes and 3-alkoxybutyraldehydes. Liebigs Ann /Recueil 1995, 1995, 29. <http://dx.doi.org/10.1002/jlac.199519950107>
  • Bergdahl Mikael, Hett Robert, Friebe Timothy L., Gangloff Anthony R., Iqbal Javed, Wu Yinghui, Helquist Paul: Synthesis of the oxazole- and diene-containing C9–C23 fragment of the type a streptogramin antibiotics. Tetrahetron Lett 1993, 34, 7371. <http://dx.doi.org/10.1016/S0040-4039(00)60128-4>
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  • Mahler Ulrike, Devant Ralf M., Braun Manfred: Reagent-controlled addition of (R)- and (S)-2-Hydroxy-1,2,2-triphenylethyl acetate to chiral aldehydes. Chem Ber 1988, 121, 2035. <http://dx.doi.org/10.1002/cber.19881211122>
  • Braun Manfred: Stereoselektive Aldolreaktionen mit α-unsubstituierten chiralen Enolaten. Angew Chem 1987, 99, 24. <http://dx.doi.org/10.1002/ange.19870990106>
  • Connell Richard, Scavo Frank, Helquist Paul, Åkermark Björn: Functionalized oxazoles from rhodiumi-catalyzed reaction of dimethyl diazomalonate with nitriles. Tetrahetron Lett 1986, 27, 5559. <http://dx.doi.org/10.1016/S0040-4039(00)85265-X>
  • Reetz Manfred T.: Chelat- oder Nicht-Chelat-Kontrolle bei Additionsreaktionen von chiralen α- und β-Alkoxycarbonyl-Verbindungen. Angew Chem 1984, 96, 542. <http://dx.doi.org/10.1002/ange.19840960805>
  • Reetz Manfred T.: Chelation or Non-Chelation Control in Addition Reactions of Chiral α- and β- Alkoxy Carbonyl Compounds [New Synthetic Methods (44)]. Angew Chem Int Ed Engl 1984, 23, 556. <http://dx.doi.org/10.1002/anie.198405561>