Michael Müller

First published: 03 January 2012

https://doi.org/10.1002/anie.201107517

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“My favorite place on earth is where my family is. My best investment was a Colnago racing bike. …︁” This and more about Michael Müller can be found on page 1514.

References

1“Highly Regio- and Enantioselective Reduction of 3,5-Dioxocarboxylates”: M. Wolberg, W. Hummel, C. Wandrey, M. Müller, Angew. Chem. 2000, 112, 4476–4478;
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Angew. Chem. Int. Ed. 2000, 39, 4306–4308. (Starting point towards the development of polyketide synthesis without using PKS.)
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2“Development of a Donor–Acceptor Concept for Catalytic Asymmetric Cross-Coupling Reactions of Aldehydes: The First Asymmetric Cross-Benzoin Condensation”: P. Dünkelmann, D. Kolter-Jung, A. Nitsche, A. S. Demir, P. Siegert, B. Lingen, M. Baumann, M. Pohl, M. Müller, J. Am. Chem. Soc. 2002, 124, 12084–12085. (Establishment of the catalytic asymmetric cross-benzoin condensation 120 years after Emil Fischer’s first report on this reaction.)
10.1021/ja0271476
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3“Unselective Phenolic Coupling of Methyl 2-Hydroxy-4-methoxy-6-methylbenzoate—A Valuable Tool for the Total Synthesis of Natural Product Families”: D. Drochner, W. Hüttel, M. Nieger, M. Müller, Angew. Chem. 2003, 115, 961–963;
10.1002/ange.200390216
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Angew. Chem. Int. Ed. 2003, 42, 931–933. (Biomimetic diversity-oriented organic synthesis of a range of different natural products.)
10.1002/anie.200390247
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4“The Enzymatic Asymmetric Conjugate Umpolung Reaction”: C. Dresen, M. Richter, M. Pohl, S. Lüdeke, M. Müller, Angew. Chem. 2010, 122, 6750–6753;
10.1002/ange.201000632
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Angew. Chem. Int. Ed. 2010, 49, 6600–6603. (Development of an enzymatic asymmetric Stetter reaction.)
10.1002/anie.201000632
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5“Diversity-Oriented Production of Metabolites Derived from Chorismate and Their Use in Organic Synthesis”: J. Bongaerts et al., Angew. Chem. 2011, 123, 7927–7932;
10.1002/ange.201103261
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Angew. Chem. Int. Ed. 2011, 50, 7781–7786. (Biogenic use of a metabolic branching point in the biosynthesis of different metabolites for the microbial production of several natural and “nonnatural” products.)
10.1002/anie.201103261
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Volume51, Issue7

February 13, 2012

Page 1514

Michael Müller

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