Financial support from the Swedish Research Council is acknowledged.
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Mechanism of Diphenylprolinol Silyl Ether Catalyzed Michael Addition Revisited—but Still Controversial†
Article first published online: 3 JAN 2013
DOI: 10.1002/anie.201207775
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
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How to Cite
Moberg, C. (2013), Mechanism of Diphenylprolinol Silyl Ether Catalyzed Michael Addition Revisited—but Still Controversial . Angew. Chem. Int. Ed., 52: 2160–2162. doi: 10.1002/anie.201207775
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Publication History
- Issue published online: 13 FEB 2013
- Article first published online: 3 JAN 2013
- Manuscript Received: 26 SEP 2012
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- Swedish Research Council
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- 1, , , , A Rational Approach Towards a New Ferrocenyl Pyrrolidine for Stereoselective Enamine Catalysis, Chemistry - A European Journal, 2013, 19, 24Direct Link:
- 2, , , , , , , , , , , , Stoichiometric Reactions of Enamines Derived from Diphenylprolinol Silyl Ethers with Nitro Olefins and Lessons for the Corresponding Organocatalytic Conversions – a Survey, Helvetica Chimica Acta, 2013, 96, 5Direct Link:

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