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Angewandte Chemie International Edition
Article . 2016 . Peer-reviewed
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Angewandte Chemie
Article . 2016 . Peer-reviewed
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King Abdullah University of Science and Technology: KAUST Repository
Article . 2016
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Catalytic Asymmetric Piancatelli Rearrangement: Brønsted Acid Catalyzed 4π Electrocyclization for the Synthesis of Multisubstituted Cyclopentenones
Authors: Yunfei Cai; Iuliana Atodiresei; Yurong Tang; Magnus Rueping; Magnus Rueping;
Catalytic Asymmetric Piancatelli Rearrangement: Brønsted Acid Catalyzed 4π Electrocyclization for the Synthesis of Multisubstituted Cyclopentenones
Abstract
AbstractThe first catalytic asymmetric Piancatelli reaction is reported. Catalyzed by a chiral Brønsted acid, the rearrangement of a wide range of furylcarbinols with a series of aniline derivatives provides valuable aminocyclopentenones in high yields as well as excellent enantioselectivities and diastereoselectivities. The high value of the aza‐Piancatelli rearrangement was demonstrated by the synthesis of a cyclopentane‐based hNK1 antagonist analogue.
Country
Saudi Arabia
Related Organizations
- King Abdullah University of Science and Technology Saudi Arabia
- RWTH Aachen University Germany
- King Abdullah University of Science and Technology Saudi Arabia
Keywords
quaternary stereocenters, rearrangements, Brønsted acids, organocatalysis, alcohols
quaternary stereocenters, rearrangements, Brønsted acids, organocatalysis, alcohols
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Fields of Science
Fields of Science