Chiral phase-transfer catalysis in the asymmetric α-heterofunctionalization of prochiral nucleophiles

Scholarly Works

• Lee, H.-J.; Maruoka, K. Asymmetric phase-transfer catalysis. Nature reviews. Chemistry 2024, 8, 851–869. doi:10.1038/s41570-024-00642-x
• Kayukova, L.; Vologzhanina, A. A New 2-Aminospiropyrazolylammonium Cation with Possible Uses in the Topical Areas of Ionic Liquids. Molecules (Basel, Switzerland) 2024, 29, 2326. doi:10.3390/molecules29102326
• Piringer, M.; Stockhammer, L.; Vogl, L.; Weinzierl, D.; Zebrowski, P.; Waser, M. Enantioselective α-heterofunctionalization reactions of catalytically generated C1-Lewis base enolates. Tetrahedron chem 2024, 9, 100063. doi:10.1016/j.tchem.2024.100063
• Xiong, T.-Z.; Yisimayili, N.; Lu, C.-D. Stereoselective Electrophilic Chlorination of β,β-Disubstituted Enesulfinamides with Chloramine-T: Asymmetric Synthesis of Acyclic α,α-Disubstituted α-Chlorinated Carbonyl Surrogates. Organic letters 2024, 26, 1851–1856. doi:10.1021/acs.orglett.4c00059
• Li, Z.; Wang, B.; Zhang, C.; Lo, W. Y.; Yang, L.; Sun, J. Catalytic Enantioselective Nucleophilic α-Chlorination of Ketones with NaCl. Journal of the American Chemical Society 2024, 146, 2779–2788. doi:10.1021/jacs.3c12826
• Zhang, J.; Song, M.; Tang, W.; Xue, D.; Xiao, J.; Sun, H.; Wang, C. Transforming Racemic Compounds into Two New Enantioenriched Chiral Products via Intermediate Kinetic Resolution. ACS Catalysis 2023, 13, 15603–15610. doi:10.1021/acscatal.3c04599
• Düfert, A. Organokatalyse. Organische Synthesemethoden; Springer Berlin Heidelberg, 2023; pp 789–845. doi:10.1007/978-3-662-65244-2_8
• Albanese, D. C. M.; Penso, M. New Trends in Asymmetric Phase Transfer Catalysis. European Journal of Organic Chemistry 2023, 26. doi:10.1002/ejoc.202300224
• Lopat'eva, E. R.; Krylov, I. B.; Lapshin, D. A.; Terent'ev, A. O. Redox-active molecules as organocatalysts for selective oxidative transformations - an unperceived organocatalysis field. Beilstein journal of organic chemistry 2022, 18, 1672–1695. doi:10.3762/bjoc.18.179
• Otevrel, J.; Waser, M. doi:10.1002/9783527832217.ch3
• Iribarren, I.; Trujillo, C. Efficiency and Suitability when Exploring the Conformational Space of Phase-Transfer Catalysts. Journal of chemical information and modeling 2022, 62, 5568–5580. doi:10.1021/acs.jcim.2c00934
• Waser, M.; Winter, M.; Mairhofer, C. (Thio)urea Containing Chiral Ammonium Salt Catalysts. Chemical record (New York, N.Y.) 2022, 23, e202200198. doi:10.1002/tcr.202200198
• Han, J.; Hoteite, L.; Harrity, J. P. A. Development of an Enantioselective Allylic Alkylation of Acyclic α-Fluoro-β-ketoesters for Asymmetric Synthesis of 3-Fluoropiperidines. Chemistry (Weinheim an der Bergstrasse, Germany) 2022, 28, e202201595. doi:10.1002/chem.202201595
• Miller, E.; Moon, P. J.; Toste, F. D. doi:10.1002/9781119736424.ch4
• Fustero, S.; Remete, A. M.; Kiss, L.; Medio‐Simón, M.; Escorihuela, J.; Sedgwick, D. M. doi:10.1002/9781119736424.ch13
• Lee, S.; Chung, W. Enantioselective halogenation via asymmetric phase‐transfer catalysis. Bulletin of the Korean Chemical Society 2022, 43, 896–911. doi:10.1002/bkcs.12546
• Liang, H.; Li, Z.; Liu, Y.; Murayama, S.; Naka, H.; Maruoka, K. Synthesis of optically pure, deuterated Maruoka Catalysts and their chemical reactivity. Tetrahedron Letters 2022, 96, 153753. doi:10.1016/j.tetlet.2022.153753
• Remete, A. M.; Nonn, M.; Escorihuela, J.; Fustero, S.; Kiss, L. Asymmetric Methods for Carbon-Fluorine Bond Formation. European Journal of Organic Chemistry 2021, 2021, 5946–5974. doi:10.1002/ejoc.202101094
• Zebrowski, P.; Eder, I.; Eitzinger, A.; Mallojjala, S. C.; Waser, M. Enantioselective Catalytic Synthesis of α-Halogenated α-Aryl-β2,2-amino Acid Derivatives. ACS organic & inorganic Au 2021, 2, 34–43. doi:10.1021/acsorginorgau.1c00025
• Zebrowski, P.; Eder, I.; Eitzinger, A.; Mallojjala, S. C.; Waser, M.

Explore citations to this article at