Ciril Jimeno
Affiliations: | Institute of Advanced Chemistry of Catalonia (IQAC-CSIC) |
Area:
organic chemistry, organocatalysis, asymmetric catalysisGoogle:
"Ciril Jimeno"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Miquel A. Pericàs | grad student | ||
| Philippe Renaud | post-doc | ||
| Patrick J. Walsh | post-doc |
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Publications
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| Sors-Vendrell A, Ortiz A, Meneses D, et al. (2022) A Degenerate Metal-Templated Catalytic System with Redundant Functional Groups for the Asymmetric Aldol Reaction. The Journal of Organic Chemistry. 87: 7509-7513 |
| Jimeno C. (2021) Amino Acylguanidines as Bioinspired Catalysts for the Asymmetric Aldol Reaction. Molecules (Basel, Switzerland). 26 |
| Solà J, Jimeno C, Alfonso I. (2020) Exploiting complexity to implement function in chemical systems. Chemical Communications (Cambridge, England) |
| Serra-Pont A, Alfonso I, Solà J, et al. (2019) An efficient dynamic asymmetric catalytic system within a zinc-templated network. Chemical Communications (Cambridge, England) |
| Serra-Pont A, Alfonso I, Solà J, et al. (2017) A copper-templated, bifunctional organocatalyst: a strongly cooperative dynamic system for the aldol reaction. Organic & Biomolecular Chemistry |
| Jimeno C. (2016) Water in asymmetric organocatalytic systems: a global perspective. Organic & Biomolecular Chemistry. 14: 6147-64 |
| Günler ZI, Companyó X, Alfonso I, et al. (2016) Deciphering the roles of multiple additives in organocatalyzed Michael additions. Chemical Communications (Cambridge, England). 52: 6821-4 |
| Jimeno C, Cao L, Renaud P. (2016) Trichloromethanesulfonyl chloride: a chlorinating reagent for aldehydes. The Journal of Organic Chemistry |
| Jimeno C, Pericàs M, Günler Z, et al. (2016) Concentration Effect in the Asymmetric Michael Addition of Acetone to β-Nitrostyrenes Catalyzed by Primary Amine Thioureas Synthesis. 49: 319-325 |
| Serra-Pont A, Alfonso I, Jimeno C, et al. (2015) Dynamic assembly of a zinc-templated bifunctional organocatalyst in the presence of water for the asymmetric aldol reaction. Chemical Communications (Cambridge, England) |