Enantioselective Michael Addition of Aldehydes to β-Nitrostyrenes Catalyzed by (S)-N -(D-Prolyl)-1-triflicamido-3-phenylpropan-2-amine
Author:
Affiliation:
1. Department of Chemistry; Indian Institute of Technology Kanpur; Kanpur Uttar Pradesh 208016 India
2. Centre for Environmental Science and Engineering; Indian Institute of Technology Kanpur; Kanpur Uttar Pradesh 208016 India
Funder
Science and Engineering Research Board
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201900719/fullpdf
Reference52 articles.
1. Efficient Proline-Catalyzed Michael Additions of Unmodified Ketones to Nitro Olefins
2. Catalytic Direct Asymmetric Michael Reactions: Taming Naked Aldehyde Donors
3. Organocatalytic Direct Michael Reaction of Ketones and Aldehydes with β-Nitrostyrene in Brine
4. Dendrimers or Nanoparticles as Supports for the Design of Efficient and Recoverable Organocatalysts?
5. Epiandrosterone-derived prolinamide as an efficient asymmetric catalyst for Michael addition reactions of aldehydes to nitroalkenes
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2. Organocatalysis for the Asymmetric Michael Addition of Aldehydes and α,β-Unsaturated Nitroalkenes;Catalysts;2022-01-20
3. Enantioselective Organocatalytic Michael Addition Reactions Catalyzed by Proline/Prolinol/Supported Proline based Organocatalysts: An Overview;ChemistrySelect;2022-01-07
4. Stereoselective Aldol and Conjugate Addition Reactions Mediated by Proline‐Based Catalysts and Its Analogues: A Concise Review;European Journal of Organic Chemistry;2021-10-04
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