Supporting Information
Deposition Numbers 2158046 (for 9a), 2170881 (for 10c) and 2170877 (for 16) contain the supplementary crystallographic data for this paper. These data are provided free of charge by the joint Cambridge Crystallographic Data Centre (http://www.ccdc.cam.ac.uk/structures) and Fachinformationszentrum Karlsruhe Access Structures service.
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Cite the Following Article
Facile and diastereoselective arylation of the privileged 1,4-dihydroisoquinolin-3(2H)-one scaffold
Dmitry Dar’in, Grigory Kantin, Alexander Bunev and Mikhail Krasavin
Beilstein J. Org. Chem. 2022, 18, 1070–1078.
https://doi.org/10.3762/bjoc.18.109
How to Cite
Dar’in, D.; Kantin, G.; Bunev, A.; Krasavin, M. Beilstein J. Org. Chem. 2022, 18, 1070–1078. doi:10.3762/bjoc.18.109
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Scholarly Works
- Guranova, N.; Bakulina, O.; Kantin, G.; Dar'in, D. Concise Approach towards Tetramic Acid Derivatives via Ugi Reaction/Dieckmann Cyclization Sequence. ChemistrySelect 2024, 9. doi:10.1002/slct.202303869
- Levashova, E.; Adamchik, M.; Kantin, G.; Dar'in, D. Chemo- and Diastereoselective Entries into All-Carbon α-Quaternary Aldehydes via C-C Insertion of 4-Diazoisoquinolin-3-ones into C-CHO Bonds. The Journal of organic chemistry 2023, 88, 11217–11226. doi:10.1021/acs.joc.3c01222
