Leito I - Search Results

1

Design of Novel Uncharged Organic Superbases: Merging Basicity and Functionality.

Vazdar K, Margetić D, Kovačević B, Sundermeyer J, Leito I, Jahn U. Vazdar K, et al. Among authors: leito i. Acc Chem Res. 2021 Aug 3;54(15):3108-3123. doi: 10.1021/acs.accounts.1c00297. Epub 2021 Jul 26. Acc Chem Res. 2021. PMID: 34308625

2

Very strong organosuperbases formed by combining imidazole and guanidine bases: synthesis, structure, and basicity.

Vazdar K, Kunetskiy R, Saame J, Kaupmees K, Leito I, Jahn U. Vazdar K, et al. Among authors: leito i. Angew Chem Int Ed Engl. 2014 Jan 27;53(5):1435-8. doi: 10.1002/anie.201307212. Epub 2013 Dec 13. Angew Chem Int Ed Engl. 2014. PMID: 24339377

3

Fluoro- and perfluoralkylsulfonylpentafluoroanilides: synthesis and characterization of NH acids for weakly coordinating anions and their gas-phase and solution acidities.

Kögel JF, Linder T, Schröder FG, Sundermeyer J, Goll SK, Himmel D, Krossing I, Kütt K, Saame J, Leito I. Kögel JF, et al. Among authors: leito i. Chemistry. 2015 Apr 7;21(15):5769-82. doi: 10.1002/chem.201405391. Epub 2015 Feb 26. Chemistry. 2015. PMID: 25727401

4

Basicity Limits of Neutral Organic Superbases.

Leito I, Koppel IA, Koppel I, Kaupmees K, Tshepelevitsh S, Saame J. Leito I, et al. Angew Chem Int Ed Engl. 2015 Aug 3;54(32):9262-5. doi: 10.1002/anie.201503345. Epub 2015 Jun 18. Angew Chem Int Ed Engl. 2015. PMID: 26088063

5

Experimental Basicities of Phosphazene, Guanidinophosphazene, and Proton Sponge Superbases in the Gas Phase and Solution.

Kaljurand I, Saame J, Rodima T, Koppel I, Koppel IA, Kögel JF, Sundermeyer J, Köhn U, Coles MP, Leito I. Kaljurand I, et al. Among authors: leito i. J Phys Chem A. 2016 Apr 28;120(16):2591-604. doi: 10.1021/acs.jpca.6b01552. Epub 2016 Apr 19. J Phys Chem A. 2016. PMID: 27093092

6

Guanidinophosphazenes: design, synthesis, and basicity in THF and in the gas phase.

Kolomeitsev AA, Koppel IA, Rodima T, Barten J, Lork E, Röschenthaler GV, Kaljurand I, Kütt A, Koppel I, Mäemets V, Leito I. Kolomeitsev AA, et al. Among authors: leito i. J Am Chem Soc. 2005 Dec 21;127(50):17656-66. doi: 10.1021/ja053543n. J Am Chem Soc. 2005. PMID: 16351095

7

Basicity of Very Weak Bases in 1,2-Dichloroethane.

Kaupmees K, Järviste R, Leito I. Kaupmees K, et al. Among authors: leito i. Chemistry. 2016 Nov 21;22(48):17445-17449. doi: 10.1002/chem.201602629. Epub 2016 Oct 21. Chemistry. 2016. PMID: 27766685

8

A unified view to Brønsted acidity scales: do we need solvated protons?

Paenurk E, Kaupmees K, Himmel D, Kütt A, Kaljurand I, Koppel IA, Krossing I, Leito I. Paenurk E, et al. Among authors: leito i. Chem Sci. 2017 Oct 1;8(10):6964-6973. doi: 10.1039/c7sc01424d. Epub 2017 Aug 7. Chem Sci. 2017. PMID: 29147523 Free PMC article.

9

Inducing a pH-dependent conformational response by competitive binding to Zn²⁺ of a series of chiral ligands of disparate basicity.

Wootten MM, Le Bailly BAF, Tshepelevitsh S, Leito I, Clayden J. Wootten MM, et al. Among authors: leito i. Chem Sci. 2022 Jan 17;13(8):2258-2269. doi: 10.1039/d1sc06812a. eCollection 2022 Feb 23. Chem Sci. 2022. PMID: 35310487 Free PMC article.

10

Basicity of some P1 phosphazenes in water and in aqueous surfactant solution.

Sooväli L, Rodima T, Kaljurand I, Kütt A, Koppel IA, Leito I. Sooväli L, et al. Among authors: leito i. Org Biomol Chem. 2006 Jun 7;4(11):2100-5. doi: 10.1039/b602797k. Epub 2006 Apr 18. Org Biomol Chem. 2006. PMID: 16729124

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