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Dual Catalysis Becomes Diastereodivergent

MPS-Authors
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Oliveira,  M. T.
Research Group Maulide, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Luparia,  M.
Research Group Maulide, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Audisio,  Davide
Research Group Maulide, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Maulide,  Nuno
Research Group Maulide, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Citation

Oliveira, M. T., Luparia, M., Audisio, D., & Maulide, N. (2013). Dual Catalysis Becomes Diastereodivergent. Angewandte Chemie International Edition: a journal of the Gesellschaft Deutscher Chemiker, 52(50), 13149-13152. doi:10.1002/anie.201305933.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0018-B2DB-6
Abstract
Diastereodivergent is cool: The development of catalytic systems able to generate each and every one of the possible product diastereoisomers from the same starting materials (i.e., that are “diastereodivergent”) is an emerging field in asymmetric catalysis. The possibility of designing such systems in a rational manner based on dual catalysis has now become reality.