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5‐(Pyrrolidin‐2‐yl)tetrazole‐Catalyzed Aldol and Mannich Reactions: Acceleration and Lower Catalyst Loading in a Continuous‐Flow Reactor
Authors:Arjan Odedra Dr  Peter?H Seeberger Prof?Dr
Institution:Laboratory for Organic Chemistry, Swiss Federal Institute of Technology (ETH) Zurich, Wolfgang‐Pauli‐Strasse 10, 8093 Zurich (Switzerland), Fax: (+41)?446‐331‐235 http://www.seeberger.ethz.ch
Abstract:Continuous organocatalysis : Fast aldol and Mannich reactions require less catalyst when conducted in a microreactor. A proline tetrazole derivative (5–10 mol %) catalyzes asymmetric aldol reactions between various aromatic aldehydes and ketones in microreactor at 60 °C with reaction times ranging from 10 to 30 min.
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Keywords:aldol reaction  asymmetric catalysis  continuous‐flow reactors  microreactors  organocatalysis
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