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Highly stereoselective hydrogenations—As key‐steps in the total synthesis of statins
Authors:Natalia Andrushko  Vasyl Andrushko  Vitali Tararov  Andrei Korostylev  Gerd König  Armin Börner
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
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.
Keywords:drug synthesis  atorvastatin  rosuvastatin  asymmetric hydrogenation  enantioselectivity  stereoselectivity  statins  asymmetric catalysis
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