Cite the Following Article
Halides as versatile anions in asymmetric anion-binding organocatalysis
Lukas Schifferer, Martin Stinglhamer, Kirandeep Kaur and Olga García Macheño
Beilstein J. Org. Chem. 2021, 17, 2270–2286.
https://doi.org/10.3762/bjoc.17.145
How to Cite
Schifferer, L.; Stinglhamer, M.; Kaur, K.; Macheño, O. G. Beilstein J. Org. Chem. 2021, 17, 2270–2286. doi:10.3762/bjoc.17.145
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Presentation Graphic
Picture with graphical abstract, title and authors for social media postings and presentations. | ||
Format: PNG | Size: 13.1 MB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Benítez, M.; Matador, E.; Velázquez, M.; Lassaletta, J. M.; Fernández, R.; Monge, D. Organocatalytic Applications of Sulfonyl Squaramides in Anion‐Recognition Strategies. European Journal of Organic Chemistry 2024. doi:10.1002/ejoc.202400837
- Pérez-Sánchez, J. C.; Herrera, R. P.; Gimeno, M. C. The Potential of Self-Activating Au(I) Complexes in Gold Catalysis. Chemistry (Weinheim an der Bergstrasse, Germany) 2024, 30, e202401825. doi:10.1002/chem.202401825
- Alemán, J.; Humbrías-Martín, J.; Del Río-Rodríguez, R.; Aguilar-Galindo, F.; Díaz-Tendero, S.; Fernández-Salas, J. A. Bicarbonate-binding catalysis for the enantioselective desymmetrization of keto sulfonium salts. Nature communications 2024, 15, 4727. doi:10.1038/s41467-024-48832-x
- 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
- Manna, A.; Joshi, H.; Singh, V. K. Organocatalytic Asymmetric Direct Vinylogous Michael Initiated Ring Closure Reaction of 4-Nitroisoxazole Derivatives to 3-Isopropylidene Oxindoles. The Journal of organic chemistry 2023, 88, 15937–15946. doi:10.1021/acs.joc.3c02125
- Šivickytė, O.; Costa, P. J. Intrinsic bond strength index as a halogen bond interaction energy predictor. Physical chemistry chemical physics : PCCP 2023, 25, 17535–17546. doi:10.1039/d2cp04786a
- Zhu, M.; Jiang, H.; Sharanov, I.; Irran, E.; Oestreich, M. Atropselektive Silylierung von 1,1′‐Biaryl‐2,6‐diolen mittels chiraler gegenaniondirigierter Desymmetrisierung und anschließender Verbesserung durch kinetische Racematspaltung. Angewandte Chemie 2023, 135. doi:10.1002/ange.202304475
- Zhu, M.; Jiang, H.-J.; Sharanov, I.; Irran, E.; Oestreich, M. Atroposelective Silylation of 1,1'-Biaryl-2,6-diols by a Chiral Counteranion Directed Desymmetrization Enhanced by a Subsequent Kinetic Resolution. Angewandte Chemie (International ed. in English) 2023, 62, e202304475. doi:10.1002/anie.202304475
- Aleksiev, M.; García Mancheño, O. Enantioselective dearomatization reactions of heteroarenes by anion-binding organocatalysis. Chemical communications (Cambridge, England) 2023, 59, 3360–3372. doi:10.1039/d2cc07101k
- Adili, A.; Webster, J.-P.; Zhao, C.; Mallojjala, S. C.; Romero-Reyes, M. A.; Ghiviriga, I.; Abboud, K. A.; Vetticatt, M. J.; Seidel, D. Mechanism of a Dually Catalyzed Enantioselective Oxa-Pictet-Spengler Reaction and the Development of a Stereodivergent Variant. ACS catalysis 2023, 13, 2240–2249. doi:10.1021/acscatal.2c05484
- Samha, M. H.; Wahlman, J. L. H.; Read, J. A.; Werth, J.; Jacobsen, E. N.; Sigman, M. S. Exploring Structure-Function Relationships of Aryl Pyrrolidine-Based Hydrogen-Bond Donors in Asymmetric Catalysis Using Data-Driven Techniques. ACS catalysis 2022, 12, 14836–14845. doi:10.1021/acscatal.2c04824
- Adili, A.; Sole, A. V.; Seidel, D.; Das, B.; Matter, M. E. N-Fluorenyltryptamines as a Useful Platform for Catalytic Enantioselective Pictet–Spengler Reactions. Synthesis 2022, 55, 1724–1735. doi:10.1055/a-1970-4452
- Shennan, B. D. A.; Berheci, D.; Crompton, J. L.; Davidson, T. A.; Field, J. L.; Williams, B. A.; Dixon, D. J. Branching out: redox strategies towards the synthesis of acyclic α-tertiary ethers. Chemical Society reviews 2022, 51, 5878–5929. doi:10.1039/d1cs00669j
- Abdurakhmanova, E. R.; Cmoch, P.; Szumna, A. Three modes of interactions between anions and phenolic macrocycles: a comparative study. Organic & biomolecular chemistry 2022, 20, 5095–5103. doi:10.1039/d2ob00880g
- Mancheño, O. G.; Entgelmeier, L.-M. Activation Modes in Asymmetric Anion-Binding Catalysis. Synthesis 2022, 54, 3907–3927. doi:10.1055/a-1846-6139
- Šebesta, R. New advances in asymmetric organocatalysis. Beilstein journal of organic chemistry 2022, 18, 240–242. doi:10.3762/bjoc.18.28
- Kutateladze, D. A.; Jacobsen, E. N. Cooperative Hydrogen-Bond-Donor Catalysis with Hydrogen Chloride Enables Highly Enantioselective Prins Cyclization Reactions. Journal of the American Chemical Society 2021, 143, 20077–20083. doi:10.1021/jacs.1c10890
- Segovia, C.; Nocquet, P.-A.; Levacher, V.; Brière, J.-F.; Oudeyer, S. Organocatalysis: A Tool of Choice for the Enantioselective Nucleophilic Dearomatization of Electron-Deficient Six-Membered Ring Azaarenium Salts. Catalysts 2021, 11, 1249. doi:10.3390/catal11101249