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- W1984559520 abstract "The thermolysis of 5-aryloxythiatriazoles 1 in the presence of norbornene (2a) and trans-cyclooctene (trans-2b) affords the corresponding thiiranes 3a and trans-3b in moderate yields. First-order kinetics are observed, suggesting that a sulfur intermediate, presumably dinitrogen sulfide, is generated in the fragmentation process of 1, which then serves as the active sulfur atom donor." @default.
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- W1984559520 date "2001-05-01" @default.
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- W1984559520 title "Episulfidation of Strained Cycloalkenes in the Thermolysis of 5-Aryloxy-1,2,3,4-thiatriazoles" @default.
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- W1984559520 doi "https://doi.org/10.1002/1099-0690(200105)2001:10<1959::aid-ejoc1959>3.0.co;2-n" @default.
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