The convergent synthesis of CI-981, an optically active, highly potent, tissue selective inhibitor of HMG-CoA reductase
- 1 April 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (17) , 2283-2284
- https://doi.org/10.1016/s0040-4039(00)74190-6
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Inhibitors of cholesterol biosynthesis. 3. Tetrahydro-4-hydroxy-6-[2-(1H-pyrrol-1-yl)ethyl]-2H-pyran 2-one inhibitors of HMG-CoA reductase. 2. Effects of introducing substituents at positions three and four of the pyrrole nucleusJournal of Medicinal Chemistry, 1991
- Hep-G2 cells and primary rat hepatocytes differ in their response to inhibitors of HMG-CoA reductaseBiochemical and Biophysical Research Communications, 1990
- Catalyzed Addition of Aldehydes to Activated Double Bonds—A New Synthetic ApproachAngewandte Chemie International Edition in English, 1976
- Synthese von Thiophen‐ und PyrrolderivatenEuropean Journal of Inorganic Chemistry, 1885
- Einwirkung des Diacetbernsteinsäureesters auf Ammoniak und primäre AminbasenEuropean Journal of Inorganic Chemistry, 1885