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  Catalytic Asymmetric Epoxidation of 2-Cyclopentenones

Lee, A., Reisinger, C. M., & List, B. (2012). Catalytic Asymmetric Epoxidation of 2-Cyclopentenones. Advanced Synthesis & Catalysis, 354(9), 1701-1706. doi:10.1002/adsc.201200072.

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 Creators:
Lee, Anna1, Author              
Reisinger, Corinna M.1, Author              
List, Benjamin1, Author              
Affiliations:
1Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, DE, ou_1445585              

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Free keywords: asymmetric catalysis; 2-cyclopentenones; epoxidation; organocatalysis; Weitz–Scheffer epoxidation
 Abstract: The first highly efficient asymmetric epoxidation of 2-cyclopentenones has been developed. Using a newly designed and readily available Cinchona amine catalyst, 2-cyclopentenones are reacted with hydrogen peroxide to give the corresponding epoxycyclopentanones in high yields and excellent enantioselectivities.

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Language(s): eng - English
 Dates: 2012-01-262012-01-262012-06-052012-06-18
 Publication Status: Published in print
 Pages: 6
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1002/adsc.201200072
 Degree: -

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Title: Advanced Synthesis & Catalysis
  Abbreviation : Adv. Synth. Catal.
Source Genre: Journal
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Publ. Info: Weinheim, Fed. Rep. of Germany : Wiley-VCH Verlag GmbH
Pages: - Volume / Issue: 354 (9) Sequence Number: - Start / End Page: 1701 - 1706 Identifier: ISSN: 1615-4150
CoNE: https://pure.mpg.de/cone/journals/resource/958634688013