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Pure Appl. Chem., 1973, Vol. 33, No. 1, pp. 1-16

http://dx.doi.org/10.1351/pac197333010001

Some aspects of the chemistry of penicillin

D. H. R. Barton

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  • Barton Derek H.R., Launay Franck: The selective functionalization of saturated hydrocarbons. Part 40. Aspects of FeII based peroxide fragmentation in pyridine solution. Tetrahedron 1997, 53, 14565. <http://dx.doi.org/10.1016/S0040-4020(97)01063-6>
  • Nudelman Abraham: THE CHEMISTRY OF OPTICALLY ACTIVE SULFUR COMPOUNDS PART III. Phosphorous and Sulfur and the Related Elements 1976, 2, 51. <http://dx.doi.org/10.1080/03086647608078931>
  • Tanida Hiroshi, Muneyuki Ryonosuke, Tsushima Tadahiko: Thermal transformation of 6-phenylthioacetamidopenicillin sulfoxide. Tetrahetron Lett 1975, 16, 3063. <http://dx.doi.org/10.1016/S0040-4039(00)75074-X>
  • Tanida Hiroshi, Tsuji Teruji, Tsushima Tadahiko, Ishitobi Hiroyuki, Irie Tadashi, Yano Toshisada, Matsumura Hiromu, Tori Kazuo: Transformation of penicillin sulfoxide ester into 2-halogen-substituted penicillin ester, intermediate to cepham system. Tetrahetron Lett 1975, 16, 3303. <http://dx.doi.org/10.1016/S0040-4039(00)91432-1>
  • Lattrell Rudolf, Lohaus Gerhard: Versuche zur Totalsynthese von Cephalosporinderivaten, II1) Substitutionsreaktionen antrans-3-Sulfonyloxy-2-azetidinonen. – Eine Synthese voncis-3-Acylamino-4-alkylthio-2-azetidinonen. Justus Liebigs Ann Chem 1974, 1974, 901. <http://dx.doi.org/10.1002/jlac.197419740606>
  • Lattrell Rudolf: 4-Mercapto-2-azetidinone, II1) Darstellung und Reaktionen von 4-Mercapto-2-azetidinonen. Justus Liebigs Ann Chem 1974, 1974, 1361. <http://dx.doi.org/10.1002/jlac.197419740902>
  • Ninomiya K., Shioiri T., Yamada S.: Phosphorus in organic synthesis—VII. Tetrahedron 1974, 30, 2151. <http://dx.doi.org/10.1016/S0040-4020(01)97352-1>
  • Lattrell Rudolf: Synthese von 4-Mercapto-2-azetidinonen mit α-Isopropylidenacetat-Funktionen am Stickstoff. Angew Chem 1973, 85, 983. <http://dx.doi.org/10.1002/ange.19730852208>
  • Lattrell Rudolf: Synthesis of 4-Mercapto-2-azetidinones having α-Isopropylideneacetate Groups on Nitrogen. Angew Chem Int Ed Engl 1973, 12, 925. <http://dx.doi.org/10.1002/anie.197309252>