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Pure Appl. Chem., 1996, Vol. 68, No. 3, pp. 609-612

http://dx.doi.org/10.1351/pac199668030609

Novel synthetic strategy for HMG-CoA reductase inhibitors

T. Hiyama

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  • Denmark Scott E., Liu Jack H.-C.: Kreuzkupplungen von Organosiliciumverbindungen in der Naturstoffsynthese. Angew Chem 2010, 122, 3040. <http://dx.doi.org/10.1002/ange.200905657>
  • Denmark Scott E., Liu Jack H.-C.: Silicon-Based Cross-Coupling Reactions in the Total Synthesis of Natural Products. Angew Chem Int Ed 2010, 49, 2978. <http://dx.doi.org/10.1002/anie.200905657>
  • HIYAMA T.: ChemInform Abstract: Novel Synthetic Strategy for HMG-CoA Reductase Inhibitors. ChemInform 2010, 27, no. <http://dx.doi.org/10.1002/chin.199640277>
  • Wolberg Michael, Hummel Werner, Müller Michael: Biocatalytic Reduction ofβ,δ-Diketo Esters: A Highly Stereoselective Approach to All Four Stereoisomers of a Chlorinatedβ,δ-Dihydroxy Hexanoate. Chem Eur J 2001, 7, 4562. <http://dx.doi.org/10.1002/1521-3765(20011105)7:21<4562::AID-CHEM4562>3.0.CO;2-4>
  • Suzuki Mikio, Yanagawa Yoshinobu, Iwasaki Hiroshi, Kanda Hiroyasu, Yanagihara Kazufumi, Matsumoto Hiroo, Ohara Yoshio, Yazaki Yukari, Sakoda Ryozo: First systematic chiral syntheses of two pairs of enantiomers with 3,5-dihydroxyheptenoic acid chain, associated with a potent synthetic statin NK-104. Biorg Med Chem Lett 1999, 9, 2977. <http://dx.doi.org/10.1016/S0960-894X(99)00519-3>