Cite the Following Article
Enolates ambushed – asymmetric tandem conjugate addition and subsequent enolate trapping with conventional and less traditional electrophiles
Péter Kisszékelyi and Radovan Šebesta
Beilstein J. Org. Chem. 2023, 19, 593–634.
https://doi.org/10.3762/bjoc.19.44
How to Cite
Kisszékelyi, P.; Šebesta, R. Beilstein J. Org. Chem. 2023, 19, 593–634. doi:10.3762/bjoc.19.44
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Scholarly Works
- Kisszékelyi, P.; Mudráková, B.; Cigáň, M.; Šebesta, R. Persistent guaiazulene arylmethylium ions as electrophilic traps for metal enolates. Chemical communications (Cambridge, England) 2024, 60, 3339–3342. doi:10.1039/d4cc00208c
- Tsogoeva, S. B. Catalytic multi-step domino and one-pot reactions. Beilstein journal of organic chemistry 2024, 20, 254–256. doi:10.3762/bjoc.20.25
- Reimann, S.; Adachi, S.; Subramanian, H.; Sibi, M. P. Enantioselective enolate protonations: Evaluation of achiral templates with fluxional brønsted basic substituents in conjugate addition of malononitriles. Tetrahedron 2024, 152, 133833. doi:10.1016/j.tet.2024.133833