Multigram scale synthesis of 3,4- and 3,6-dihydro-2H-thiopyran 1,1-dioxides and features of their NMR spectral behavior

Roman M. ChabanenkoDepartment of Organic Chemistry, Oles Honchar Dnipro National University, Dnipro, Ukraine; View further author information

Svitlana Yu. MykolenkoDepartment of Chemistry, Dnipro State University of Agriculture and Economics, Dnipro, UkraineView further author information

Eugene K. KozirevDepartment of Organic Chemistry, Oles Honchar Dnipro National University, Dnipro, Ukraine; View further author information

Vitalii A. PalchykovDepartment of Organic Chemistry, Oles Honchar Dnipro National University, Dnipro, Ukraine; Correspondence[email protected]

http://orcid.org/0000-0003-3748-4566 View further author information

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Nazariy T. Pokhodylo, Mykola A. Tupychak & Vitalii A. Palchykov. (2020) Dihydro-2H-thiopyran-3(4H)-one-1,1-dioxide – a new cyclic ketomethylenic reagent for the Dimroth-type 1,2,3-triazole synthesis. Synthetic Communications 50:12, pages 1835-1844.
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Alberto F. Garrido‐Castro, Yuta Hioki, Yoshifumi Kusumoto, Kyohei Hayashi, Jeremy Griffin, Kaid C. Harper, Yu Kawamata & Phil S. Baran. (2023) Scalable Electrochemical Decarboxylative Olefination Driven by Alternating Polarity**. Angewandte Chemie International Edition 62:42.
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Kateryna V. Dil, Yevhenii K. Kozyriev & Vitalii A. Palchykov. (2023) Rh-catalyzed cyclization of carbamates–synthesis of a new heterocyclic system: tetrahydro-3H-4-oxa-2-thia-2b-azacyclopropa[cd]pentalen-3-one 2,2-dioxide. Chemical Papers.
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Multigram scale synthesis of 3,4- and 3,6-dihydro-2H-thiopyran 1,1-dioxides and features of their NMR spectral behavior

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Multigram scale synthesis of 3,4- and 3,6-dihydro-2H-thiopyran 1,1-dioxides and features of their NMR spectral behavior

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