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Pure Appl. Chem., 2000, Vol. 72, No. 9, pp. 1763-1768

http://dx.doi.org/10.1351/pac200072091763

Versatility of β-lactams in synthesis. Studies directed toward the synthesis of complex nucleoside antibiotics and some macrocyclic peptides

Claudio Palomo, Jesús M. Aizpurua, Iñaki Ganboa and Mikel Oiarbide

Departamento de Química Orgánica, Facultad de Química, Universidad del País Vasco, Apdo 1072, 20080 San Sebastián, Spain

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  • Chen Jiang-Hua, Liao Sai-Hu, Sun Xiu-Li, Shen Qi, Tang Yong: Tris(oxazoline)/copper-catalyzed coupling of alkynes with nitrones: a highly enantioselective access to β-lactams. Tetrahedron 2012, 68, 5042. <http://dx.doi.org/10.1016/j.tet.2012.04.049>
  • Palomo Claudio, Aizpurua Jesus M., Ganboa Inaki, Oiarbide Mikel: ChemInform Abstract: Versatility of β-Lactams in Synthesis: Studies Directed Toward the Synthesis of Complex Nucleoside Antibiotics and Some Macrocyclic Peptides. ChemInform 2010, 32, no. <http://dx.doi.org/10.1002/chin.200123274>
  • McKay Craig S., Kennedy David C., Pezacki John Paul: Studies of multicomponent Kinugasa reactions in aqueous media. Tetrahetron Lett 2009, 50, 1893. <http://dx.doi.org/10.1016/j.tetlet.2009.02.035>
  • von Nussbaum Franz, Brands Michael, Hinzen Berthold, Weigand Stefan, Häbich Dieter: Antibakterielle Naturstoffe in der medizinischen Chemie – Exodus oder Renaissance?. Angew Chem 2006, 118, 5194. <http://dx.doi.org/10.1002/ange.200600350>
  • von Nussbaum Franz, Brands Michael, Hinzen Berthold, Weigand Stefan, Häbich Dieter: Antibacterial Natural Products in Medicinal Chemistry—Exodus or Revival?. Angew Chem Int Ed 2006, 45, 5072. <http://dx.doi.org/10.1002/anie.200600350>
  • Yang Yan, Kayser Margaret M., Rochon Fernande D., Rodríguez Sonia, Stewart Jon D.: Assessing substrate acceptance and enantioselectivity of yeast reductases in reactions with substituted α-keto β-lactams. Mol Catal B Enzym 2005, 32, 167. <http://dx.doi.org/10.1016/j.molcatb.2004.10.005>
  • Wang Fengyun, Rochon Fernande D, Kayser Margaret M, Yang Yan: Synthesis of novel optically pure β-lactams. Can J Chem 2005, 83, 28. <http://dx.doi.org/10.1139/v04-159>
  • Cainelli Gianfranco, Giacomini Daria, Gazzano Massimo, Galletti Paola, Quintavalla Arianna: N-Acylation of 4-alkylidene-β-lactams: unexpected results. Tetrahetron Lett 2003, 44, 6269. <http://dx.doi.org/10.1016/S0040-4039(03)01533-8>
  • Arjona Odón, Csákÿ Aurelio G, Murcia M.Carmen, Plumet Joaquı́n: The Staudinger reaction of imines derived from 7-oxanorbornenone: formation of spiranic oxazinone versus β-lactam rings. Tetrahetron Lett 2002, 43, 6405. <http://dx.doi.org/10.1016/S0040-4039(02)01375-8>
  • Quayle, Peter: THE CHEMISTRY ΟFTHE CARBON-TIN BOND: ANOTHER CHEMICAL CHAMELEON?. MGMC 2002, 25, 33. <http://dx.doi.org/10.1515/MGMC.2002.25.1-2.33>
  • Magriotis Plato A.: Neues über die enantioselektive Synthese vonβ-Lactamen: Entwicklung der ersten katalytischen Ansätze. Angew Chem 2001, 113, 4507. <http://dx.doi.org/10.1002/1521-3757(20011203)113:23<4507::AID-ANGE4507>3.0.CO;2-2>
  • Palomo Claudio, Oiarbide Mikel, Ganboa Iñaki, Miranda José I: A concise synthesis of α-amino acid N-carboxy anhydrides of (2S,3S)-β-substituted serines. Tetrahetron Lett 2001, 42, 8955. <http://dx.doi.org/10.1016/S0040-4039(01)01766-X>