Ambident reactivity of enolizable 5-mercapto-1H-tetrazoles in trapping reactions with in situ-generated thiocarbonyl S-methanides derived from sterically crowded cycloaliphatic thioketones

Grzegorz Mlostoń, Małgorzata Celeda, Marcin Palusiak, Heinz Heimgartner, Marta Denel-Bobrowska and Agnieszka B. Olejniczak
Beilstein J. Org. Chem. 2025, 21, 1508–1519. https://doi.org/10.3762/bjoc.21.113

Supporting Information

CCDC-2420216 and CCDC-2420217 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via http://www.ccdc.cam.ac.uk/structures.

Supporting Information File 1: General information and experimental data of all isolated products, procedure for determination of biological activity, details of the crystal structure determination, and copies of 1H and 13C NMR spectra for all products.
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Cite the Following Article

Ambident reactivity of enolizable 5-mercapto-1H-tetrazoles in trapping reactions with in situ-generated thiocarbonyl S-methanides derived from sterically crowded cycloaliphatic thioketones
Grzegorz Mlostoń, Małgorzata Celeda, Marcin Palusiak, Heinz Heimgartner, Marta Denel-Bobrowska and Agnieszka B. Olejniczak
Beilstein J. Org. Chem. 2025, 21, 1508–1519. https://doi.org/10.3762/bjoc.21.113

How to Cite

Mlostoń, G.; Celeda, M.; Palusiak, M.; Heimgartner, H.; Denel-Bobrowska, M.; Olejniczak, A. B. Beilstein J. Org. Chem. 2025, 21, 1508–1519. doi:10.3762/bjoc.21.113

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