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Reduction of Ketones with LiAlH4 Complexes of α,α,α',α'-Tetraaryl-1,3-dioxolane-4,5-dimethanols (TADDOLs) A Combination of Enantioselective Reduction and Clathrate Formation with a Discussion of LAH Reagents Bearing C2-Symmetrical Ligands

Dieter Seebach ; Laboratorium für Organische Chemie der Eidgenössischen Technischen Hochschule, ETH-Zentrum, Universitátstrasse 16, CH-8092 Zürich, Switzerland
Albert K. Beck ; Laboratorium für Organische Chemie der Eidgenössischen Technischen Hochschule, ETH-Zentrum, Universitátstrasse 16, CH-8092 Zürich, Switzerland
Robert Dahinden ; Laboratorium für Organische Chemie der Eidgenössischen Technischen Hochschule, ETH-Zentrum, Universitátstrasse 16, CH-8092 Zürich, Switzerland
Matthias Hoffmann ; Laboratorium für Organische Chemie der Eidgenössischen Technischen Hochschule, ETH-Zentrum, Universitátstrasse 16, CH-8092 Zürich, Switzerland
Florian N. M. Kühnle ; Laboratorium für Organische Chemie der Eidgenössischen Technischen Hochschule, ETH-Zentrum, Universitátstrasse 16, CH-8092 Zürich, Switzerland

Puni tekst: engleski, pdf (9 MB) str. 459-484 preuzimanja: 963* citiraj
APA 6th Edition
Seebach, D., Beck, A.K., Dahinden, R., Hoffmann, M. i Kühnle, F.N.M. (1996). Reduction of Ketones with LiAlH4 Complexes of α,α,α',α'-Tetraaryl-1,3-dioxolane-4,5-dimethanols (TADDOLs) A Combination of Enantioselective Reduction and Clathrate Formation with a Discussion of LAH Reagents Bearing C2-Symmetrical Ligands. Croatica Chemica Acta, 69 (2), 459-484. Preuzeto s https://hrcak.srce.hr/136667
MLA 8th Edition
Seebach, Dieter, et al. "Reduction of Ketones with LiAlH4 Complexes of α,α,α',α'-Tetraaryl-1,3-dioxolane-4,5-dimethanols (TADDOLs) A Combination of Enantioselective Reduction and Clathrate Formation with a Discussion of LAH Reagents Bearing C2-Symmetrical Ligands." Croatica Chemica Acta, vol. 69, br. 2, 1996, str. 459-484. https://hrcak.srce.hr/136667. Citirano 25.02.2021.
Chicago 17th Edition
Seebach, Dieter, Albert K. Beck, Robert Dahinden, Matthias Hoffmann i Florian N. M. Kühnle. "Reduction of Ketones with LiAlH4 Complexes of α,α,α',α'-Tetraaryl-1,3-dioxolane-4,5-dimethanols (TADDOLs) A Combination of Enantioselective Reduction and Clathrate Formation with a Discussion of LAH Reagents Bearing C2-Symmetrical Ligands." Croatica Chemica Acta 69, br. 2 (1996): 459-484. https://hrcak.srce.hr/136667
Harvard
Seebach, D., et al. (1996). 'Reduction of Ketones with LiAlH4 Complexes of α,α,α',α'-Tetraaryl-1,3-dioxolane-4,5-dimethanols (TADDOLs) A Combination of Enantioselective Reduction and Clathrate Formation with a Discussion of LAH Reagents Bearing C2-Symmetrical Ligands', Croatica Chemica Acta, 69(2), str. 459-484. Preuzeto s: https://hrcak.srce.hr/136667 (Datum pristupa: 25.02.2021.)
Vancouver
Seebach D, Beck AK, Dahinden R, Hoffmann M, Kühnle FNM. Reduction of Ketones with LiAlH4 Complexes of α,α,α',α'-Tetraaryl-1,3-dioxolane-4,5-dimethanols (TADDOLs) A Combination of Enantioselective Reduction and Clathrate Formation with a Discussion of LAH Reagents Bearing C2-Symmetrical Ligands. Croatica Chemica Acta [Internet]. 1996 [pristupljeno 25.02.2021.];69(2):459-484. Dostupno na: https://hrcak.srce.hr/136667
IEEE
D. Seebach, A.K. Beck, R. Dahinden, M. Hoffmann i F.N.M. Kühnle, "Reduction of Ketones with LiAlH4 Complexes of α,α,α',α'-Tetraaryl-1,3-dioxolane-4,5-dimethanols (TADDOLs) A Combination of Enantioselective Reduction and Clathrate Formation with a Discussion of LAH Reagents Bearing C2-Symmetrical Ligands", Croatica Chemica Acta, vol.69, br. 2, str. 459-484, 1996. [Online]. Dostupno na: https://hrcak.srce.hr/136667. [Citirano: 25.02.2021.]

Sažetak
A complex prepared from one equivalent each of LiAlH4, EtOH and a TADDOL (α,α,α',α'-tetraaryl-1,3-dioxolane-4,5-dimethanol) reduces aryl alkyl ketones to sec. alcohols with enantiomer ratios (er) up to 96 : 4. The chiral LAH derivative is used in two-fold excess in THF solution and at dry ice temperatures. The ability of TADDOLs to form clathrates diastereoselectively can be exploited to increase the er of the initially formed alcohols by a simple modification of the work-up procedure and hence, products of very high en- antiopurity (er 99 : 1) can be isolated. When (7i,/i)-TADDOLs (from (ZiA)-tartrate) are applied in the reaction, the 1-aryl-alkanols formed preferentially have (S) configuration, as for the products obtained with the corresponding (P)-BINOL and (P)-BIPHENOL derivatives. A common mechanistic model is discussed.

Hrčak ID: 136667

URI
https://hrcak.srce.hr/136667

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