Reductive cleavage of annulated 5,6-dihydro-2-1,2,4-thiadiazine-1,1-dioxides: medium sized ring azasultams

A novel method for synthesis of medium sized ring azasultams was proposed. It includes reductive cleavage with sodium cyanoborohydride of annulated 5,6-dihydro-2 H -1,2,4-thiadiazine-1,1-dioxides that were prepared in bulk quantities by an improved procedure consisting of reacting cyclic imidates wi...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2023-07, Vol.59 (61), p.9396-9399
Hauptverfasser: Lysenko, Viacheslav, Nazarenko, Kostiantyn, Shishkina, Svitlana, Kostyuk, Aleksandr
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container_end_page 9399
container_issue 61
container_start_page 9396
container_title Chemical communications (Cambridge, England)
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creator Lysenko, Viacheslav
Nazarenko, Kostiantyn
Shishkina, Svitlana
Kostyuk, Aleksandr
description A novel method for synthesis of medium sized ring azasultams was proposed. It includes reductive cleavage with sodium cyanoborohydride of annulated 5,6-dihydro-2 H -1,2,4-thiadiazine-1,1-dioxides that were prepared in bulk quantities by an improved procedure consisting of reacting cyclic imidates with taurine followed by treatment with phosphorus oxychloride in the presence of DIPEA. A novel method for synthesis of medium sized ring azasultams was proposed.
doi_str_mv 10.1039/d3cc02849f
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
title Reductive cleavage of annulated 5,6-dihydro-2-1,2,4-thiadiazine-1,1-dioxides: medium sized ring azasultams
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