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

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.

Supporting Information File 1: General experimental information, X-ray crystallographic data, synthetic procedures, analytical data and NMR spectra for the reported compounds.
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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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  • 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
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