Organocatalysis for the Asymmetric Michael Addition of Aldehydes and α,β-Unsaturated Nitroalkenes
Michael addition is an important reaction because it can be used to synthesize a wide range of natural products or complex compounds that exhibit biological activities. In this study, a mirror image of an aldehyde and α,β-unsaturated nitroalkene were reacted in the presence of (<i>R</i>,...
Main Authors: | Jae Ho Shim, Seok Hyun Cheun, Hyeon Soo Kim, Deok-Chan Ha |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-01-01
|
Series: | Catalysts |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4344/12/2/121 |
Similar Items
-
Organocatalysis for the Asymmetric Michael Addition of Cycloketones and <i>α</i>, <i>β</i>-Unsaturated Nitroalkenes
by: Jae Ho Shim, et al.
Published: (2021-08-01) -
Organocatalytic Asymmetric Michael Addition of Ketones to <i>α</i>, <i>β</i>-Unsaturated Nitro Compounds
by: Jae Ho Shim, et al.
Published: (2020-06-01) -
Enantioselective Organocatalyzed Michael Addition of Isobutyraldehyde to Maleimides in Aqueous Media
by: Jae Ho Shim, et al.
Published: (2022-04-01) -
Synthesis of D-Fructose-Based Bifunctional Primary Amine-Thiourea Organocatalysts and Their Applications in Asymmetric Reactions
by: Samson Lalhmangaihzuala, et al.
Published: (2023-10-01) -
Supported bifunctional thioureas as recoverable and reusable catalysts for enantioselective nitro-Michael reactions
by: José M. Andrés, et al.
Published: (2016-04-01)