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 |
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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 |
format | Article |
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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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