Organocatalysis in the Chemical Transformations
Author:
Affiliation:
1. Instituto Nacional de Metrologia, Qualidade e Tecnologia (INMETRO), Duque de Caxias 25250-020, RJ, Brazil
Abstract
Publisher
MDPI AG
Subject
Physical and Theoretical Chemistry,Catalysis,General Environmental Science
Link
https://www.mdpi.com/2073-4344/13/9/1282/pdf
Reference8 articles.
1. Spotting trends in organocatalysis for the next decade;Lassaletta;Nat. Commun.,2020
2. Zalewska, K., Pinto, I., Cabrita, L., Zakrzewska, M., Noronha, J., da Ponte, M., and Branco, L. (2023). Development of L-Proline-Based Chiral Ionic Liquids for Asymmetric Michael Reaction. Catalysts, 13.
3. Jacoby, C., Sbardelotto, J., Daitx, T., Dalberto, B., Mauler, R., and Schneider, P. (2023). Poly(ε-caprolactones) Initiated by Chiral Compounds: A New Protocol to Support Organocatalysts. Catalysts, 13.
4. Fleischer, O., Targel, T., Saady, F., and Portnoy, M. (2023). Similarities and Differences between Site-Selective Acylation and Phosphorylation of Amphiphilic Diols, Promoted by Nucleophilic Organocatalysts Decorated with Outer-Sphere Appendages. Catalysts, 13.
5. Martelli, L., Machado, I., dos Santos, J., and Corrêa, A. (2023). Recent Advances in Greener Asymmetric Organocatalysis Using Bio-Based Solvents. Catalysts, 13.
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