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- W3014784977 endingPage "5862" @default.
- W3014784977 startingPage "5838" @default.
- W3014784977 abstract "Imine and enamine bonds decorate the skeleton of numerous reagents, catalysts, and organic materials. However, it is difficult to isolate at will a single tautomer, as dynamic equilibria occur easily, even in the solid state, and are sensitive to electronic and steric effect, including π-conjugation and H-bonding. Here, using as model Schiff bases generated from salicylaldehydes and TRIS in a set of linear free energy relationships (LFER), we disclose how the formation of either imines or enamines can be controlled and provide a comprehensive framework that captures the structural underpinning of this prediction. This work highlights the potentiality of tailor-made designs en route to compounds with desirable functionality." @default.
- W3014784977 created "2020-04-10" @default.
- W3014784977 creator A5003568584 @default.
- W3014784977 creator A5030118286 @default.
- W3014784977 creator A5053386939 @default.
- W3014784977 creator A5071378609 @default.
- W3014784977 date "2020-04-07" @default.
- W3014784977 modified "2023-10-17" @default.
- W3014784977 title "Imine or Enamine? Insights and Predictive Guidelines from the Electronic Effect of Substituents in H-Bonded Salicylimines" @default.
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