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Pure Appl. Chem., 1998, Vol. 70, No. 2, pp. 339-344

http://dx.doi.org/10.1351/pac199870020339

Complete structure of maitotoxin

Y. Kishi

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  • Nicolaou K. C., Aversa Robert J.: Maitotoxin: An Inspiration for Synthesis. Isr J Chem 2011, 51, 359. <http://dx.doi.org/10.1002/ijch.201100003>
  • Mohapatra Debendra K., Das Pragna P., Pattanayak Manas Ranjan, Yadav J. S.: Iodine-Catalyzed Highly Diastereoselective Synthesis of trans-2,6-Disubstituted-3,4-Dihydropyrans: Application to Concise Construction of C28-C37 Bicyclic Core of (+)-Sorangicin A. Chem Eur J 2010, 16, 2072. <http://dx.doi.org/10.1002/chem.200902999>
  • KISHI Y.: ChemInform Abstract: Complete Structure of Maitotoxin. ChemInform 2010, 29, no. <http://dx.doi.org/10.1002/chin.199846303>
  • Nicolaou K. C., Aversa Robert J., Jin Jian, Rivas Fatima: Synthesis of the ABCDEFG Ring System of Maitotoxin. J Am Chem Soc 2010, 132, 6855. <http://dx.doi.org/10.1021/ja102260q>
  • Yu Xiuzhao, Cao Zhongyan, Zhang Junliang: Organocatalytic hetero [4+2] cycloaddition reactions of 2-(1-alkynyl)-2-alkene-1-ones: metal-free access to highly substituted 4H-pyrans. Org Biomol Chem 2010, 8, 5059. <http://dx.doi.org/10.1039/c0ob00334d>
  • Gallimore Andrew R.: The biosynthesis of polyketide-derived polycyclic ethers. Nat Prod Rep 2009, 26, 266. <http://dx.doi.org/10.1039/b807902c>
  • Rohr Kerstin, Mahrwald Rainer: Catalyst-Free Aldol Additions of 1,3-Dicarbonyl Compounds. Adv Synth Catal 2008, 350, 2877. <http://dx.doi.org/10.1002/adsc.200800554>
  • Nicolaou K. C., Frederick Michael O., Aversa Robert J.: Die Entdeckung und Synthese von marinen Polyethern. Angew Chem 2008, 120, 7292. <http://dx.doi.org/10.1002/ange.200801696>
  • Nicolaou K. C., Frederick Michael O., Aversa Robert J.: The Continuing Saga of the Marine Polyether Biotoxins. Angew Chem Int Ed 2008, 47, 7182. <http://dx.doi.org/10.1002/anie.200801696>
  • Larrosa Igor, Romea Pedro, Urpí Fèlix: Synthesis of six-membered oxygenated heterocycles through carbon–oxygen bond-forming reactions. Tetrahedron 2008, 64, 2683. <http://dx.doi.org/10.1016/j.tet.2007.11.092>
  • Murata Michio, Matsumori Nobuaki, Konoki Keiichi, Oishi Tohru: Structural Features of Dinoflagellate Toxins Underlying Biological Activity as Viewed by NMR. Bull Chem Soc Jpn 2008, 81, 307. <http://dx.doi.org/10.1246/bcsj.81.307>
  • Bartók Tibor, Szécsi Árpád, Szekeres András, Mesterházy Ákos, Bartók Mihály: Detection of new fumonisin mycotoxins and fumonisin-like compounds by reversed-phase high-performance liquid chromatography/electrospray ionization ion trap mass spectrometry. Rapid Commun Mass Spectrom 2006, 20, 2447. <http://dx.doi.org/10.1002/rcm.2607>
  • Kishi Yoshito: Palytoxin: an inexhaustible source of inspiration—personal perspective. Tetrahedron 2002, 58, 6239. <http://dx.doi.org/10.1016/S0040-4020(02)00624-5>