A novel rearrangement attending the addi
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Leo A. Paquette; Melvin Rosen
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Article
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1967
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Elsevier Science
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French
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When a sulfene is generated in the presence of an enamine, a considerable propensity for cycloaddition to a B-aminothietsne dioxide exists (1). The most obvious feature of ' N CH312 ,I M 2, e 0 CH C6H5C"S02 8 I.