1954
DOI: 10.1021/ja01640a019
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Reduction of Some Conjugated Azomethine Systems by Aryl Thiols

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1955
1955
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1982

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Cited by 10 publications
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“…This amine is a weak base (Kh 1.86 X 10~ ) and undergoes the usual amine reactions. 4-Aminotetrahydrothiapyran-l-dioxide (III), the sulfone of II, was prepared by the reduction of the oxime of tetrahydro-l,4-thiapyran-l-dioxide with hydrogen and Raney nickel in good yields. It was made also by the oxidation of an amide of II followed by hydrolysis.…”
mentioning
confidence: 99%
“…This amine is a weak base (Kh 1.86 X 10~ ) and undergoes the usual amine reactions. 4-Aminotetrahydrothiapyran-l-dioxide (III), the sulfone of II, was prepared by the reduction of the oxime of tetrahydro-l,4-thiapyran-l-dioxide with hydrogen and Raney nickel in good yields. It was made also by the oxidation of an amide of II followed by hydrolysis.…”
mentioning
confidence: 99%