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| Supporting Information File 2: Crystallographic data (CIF) for compound (S)-12e. | ||
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| Supporting Information File 3: Crystallographic data (CIF) for compound (rac)-12e. | ||
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Cite the Following Article
Controlling the stereochemistry in 2-oxo-aldehyde-derived Ugi adducts through the cinchona alkaloid-promoted electrophilic fluorination
Yuqing Wang, Gaigai Wang, Anatoly A. Peshkov, Ruwei Yao, Muhammad Hasan, Manzoor Zaman, Chao Liu, Stepan Kashtanov, Olga P. Pereshivko and Vsevolod A. Peshkov
Beilstein J. Org. Chem. 2020, 16, 1963–1973.
https://doi.org/10.3762/bjoc.16.163
How to Cite
Wang, Y.; Wang, G.; Peshkov, A. A.; Yao, R.; Hasan, M.; Zaman, M.; Liu, C.; Kashtanov, S.; Pereshivko, O. P.; Peshkov, V. A. Beilstein J. Org. Chem. 2020, 16, 1963–1973. doi:10.3762/bjoc.16.163
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Scholarly Works
- Bouzbouz, S.; Cahard, D. Oxidation: C–X Bond Formation (X = Halogen, S, Se). Comprehensive Chirality; Elsevier, 2024; pp 217–242. doi:10.1016/b978-0-32-390644-9.00027-5
- Shibata, N.; Cahard, D. N-Fluoro Ammonium Salts of Cinchona Alkaloids in Enantioselective Electrophilic Fluorination. Chemical record (New York, N.Y.) 2023, 23, e202300096. doi:10.1002/tcr.202300096
