Highly stereoselective hydrogenations—As key‐steps in the total synthesis of statins |
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Authors: | Natalia Andrushko Vasyl Andrushko Vitali Tararov Andrei Korostylev Gerd König Armin Börner |
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Affiliation: | 1. Leibniz‐Institut für Katalyse an der Universit?t Rostock e.V., 18059, Rostock, Germany;2. Ratiopharm GmbH, 89070, Ulm, Germany;3. Institut für Chemie der Universit?t Rostock, 18059, Rostock, Germany |
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Abstract: | Statins are inhibitors of 3‐hydroxy‐3‐methyl‐glutaryl coenzyme A reductase (HMG‐CoA reductase) and became the standard of care for treatment of hypercholesterolemia because of their efficacy, safety, and long‐term benefits. They are administered as diastereo‐ and enantiomerically pure compounds. We summarize here two new approaches for the total synthesis of the most important representatives, atorvastatin, and rosuvastatin, based on highly stereoselective hydrogenations as key‐steps. Chirality 2010. © 2009 Wiley‐Liss, Inc. |
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Keywords: | drug synthesis atorvastatin rosuvastatin asymmetric hydrogenation enantioselectivity stereoselectivity statins asymmetric catalysis |
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