Synthesis of New Di- and Triamides as Potential Organocatalysts for Asymmetric Aldol Reaction in Water
New di- or triamide organocatalysts derived from (L)-proline were synthesized and successfully used in the direct asymmetric aldol reaction of aliphatic ketones and aromatic aldehydes in water at 0oC in the presence of benzoic acid as co-catalyst. (S)-methyl-2-((S)-3-hydroxy-2-((S)-3-pyrrolidine-2-c...
Main Authors: | Elif Keskin, Cigdem Yolacan, Feray Aydogan |
---|---|
Format: | Article |
Language: | English |
Published: |
Slovenian Chemical Society
2020-12-01
|
Series: | Acta Chimica Slovenica |
Subjects: | |
Online Access: | https://journals.matheo.si/index.php/ACSi/article/view/4748 |
Similar Items
-
Prolinethioamides versus Prolinamides in Organocatalyzed Aldol Reactions—A Comparative Study
by: Dominika J. Pielacińska, et al.
Published: (2011-06-01) -
Asymmetric total synthesis of smyrindiol employing an organocatalytic aldol key step
by: Dieter Enders, et al.
Published: (2012-07-01) -
Bioinspired Polymer-Bound Organocatalysts for Direct Asymmetric Aldol Reaction: Experimental and Computational Studies
by: Ganhong Du, et al.
Published: (2019-04-01) -
Amino Acylguanidines as Bioinspired Catalysts for the Asymmetric Aldol Reaction
by: Ciril Jimeno
Published: (2021-02-01) -
A Simple and Efficient Protocol for Proline-Catalysed Asymmetric Aldol Reaction
by: Marco Giuseppe Emma, et al.
Published: (2020-06-01)