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Pure Appl. Chem., 1986, Vol. 58, No. 3, pp. 395-406

http://dx.doi.org/10.1351/pac198658030395

Syntheses of marine molecules

J. D. Martin, J. M. Palazon, C. Perez and J. L. Ravelo

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  • Wang Bin-Gui, Gloer James B., Ji Nai-Yun, Zhao Jian-Chun: Halogenated Organic Molecules of Rhodomelaceae Origin: Chemistry and Biology. Chem. Rev. 2013, 113, 3632. <http://dx.doi.org/10.1021/cr9002215>
  • Stamatov Stephan D., Stawinski Jacek: Regioselective and Stereospecific Halosilylating Cleavage of the Oxirane System of Glycidol Derivatives as an Efficient Strategy to C2-O-Functionalized C3-Vicinal Halohydrins. Eur J Org Chem 2008, 2008, 2635. <http://dx.doi.org/10.1002/ejoc.200800112>
  • Stamatov Stephan D., Stawinski Jacek: Regioselective and stereospecific opening of an oxirane system mediated by trifluoroacetic acid and halide anions. A new direct approach to C3-vicinal halohydrins. Tetrahetron Lett 2007, 48, 1887. <http://dx.doi.org/10.1016/j.tetlet.2007.01.083>
  • Stamatov Stephan D., Stawinski Jacek: Efficient, highly regioselective, and stereospecific conversion of glycidol systems into C2-O-acylated vicinal halohydrins. Tetrahetron Lett 2006, 47, 2543. <http://dx.doi.org/10.1016/j.tetlet.2006.02.050>
  • Palmblad Magnus, Wetterhall Magnus, Markides Karin, Håkansson Per, Bergquist Jonas: Analysis of enzymatically digested proteins and protein mixtures using a 9.4 Tesla Fourier transform ion cyclotron mass spectrometer. Rapid Commun Mass Spectrom 2000, 14, 1029. <http://dx.doi.org/10.1002/1097-0231(20000630)14:12<1029::AID-RCM984>3.0.CO;2-#>
  • De Laeter John R., De Bièvre Paul, Peiser H. S.: Isotope mass spectrometry in metrology. Mass Spectrom Rev 1992, 11, 193. <http://dx.doi.org/10.1002/mas.1280110303>
  • De Laeter John R.: Mass spectrometry in nuclear science. Mass Spectrom Rev 1988, 7, 71. <http://dx.doi.org/10.1002/mas.1280070104>