中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | (Z)-1-methyl-4-(styrylsulfonyl)benzene | 16212-08-1 | C15H14O2S | 258.341 |
对甲苯基乙烯基砜 | tolyl vinyl sulfone | 5535-52-4 | C9H10O2S | 182.243 |
—— | 4-methylphenylstyryl sulfide | 92550-70-4 | C15H14S | 226.342 |
—— | (Z)-styryl(p-tolyl)sulfane | 24182-83-0 | C15H14S | 226.342 |
对甲砜基甲苯 | Methyl p-tolyl sulfone | 3185-99-7 | C8H10O2S | 170.232 |
对甲苯磺酰氯甲烷 | chloromethyl p-tolylsulfone | 7569-26-8 | C8H9ClO2S | 204.677 |
—— | (Z)-1-(4-methylsulfonyl)-2-(phenyltelluryl)-2-phenylethene | —— | C21H18O2STe | 462.039 |
4-甲苯磺酰氰 | P-toluenesulfonyl cyanide | 19158-51-1 | C8H7NO2S | 181.215 |
1-(溴甲基磺酰基)-4-甲基苯 | bromomethyl 4-tolyl sulfone | 37891-95-5 | C8H9BrO2S | 249.128 |
A base-mediated bifunctionalization of alkenes for the synthesis of α-sulfonylethanone oximes was developed in water under metal-free conditions. This reaction features a wide substrate scope and facile starting materials to afford the desired products in high yields.