α-Oxoketene dithioacetals 2 via, 1,2-nucleophilic addition by allyl magnesium bromide afforded corresponding alcohols (3).Treated with water and catalyzed by Lewis acid, the alcohols 3 were converted regiospecificall...α-Oxoketene dithioacetals 2 via, 1,2-nucleophilic addition by allyl magnesium bromide afforded corresponding alcohols (3).Treated with water and catalyzed by Lewis acid, the alcohols 3 were converted regiospecifically to the conjugated 1,1—dialkylthio—1,3,5 hexatrienes (4). Both the alcohol 8 and its methoxy methyl ether 9 were sensative to dilute sulfuric acid and cyclized under this condition to form the aryl methylthio ether (10).展开更多
α, α′ -Dioxo (ester ) ketene cyclic S, S-acetais 2 were reacted withethyleneddriine to chrd α, α′-dioxo (ester)ketene cyclic N, N-acetals 3 Thisprocess provides a new method for the synthesis of 3 in gnd yteld u...α, α′ -Dioxo (ester ) ketene cyclic S, S-acetais 2 were reacted withethyleneddriine to chrd α, α′-dioxo (ester)ketene cyclic N, N-acetals 3 Thisprocess provides a new method for the synthesis of 3 in gnd yteld under mildcondition. All products are confirmed with elementai analpeis, IR, 1H NMR and13~C NMR展开更多
Aliphatic α-oxo ketene cyclic dithioacetals 1 were reacted with allyl magne- sium bromide to afford the 1,2-addition products 2.Catalyzed by boron trifluoride etherate,the adducts 2 were etherified by methanol to aff...Aliphatic α-oxo ketene cyclic dithioacetals 1 were reacted with allyl magne- sium bromide to afford the 1,2-addition products 2.Catalyzed by boron trifluoride etherate,the adducts 2 were etherified by methanol to afford the corresponding methyl ethers 3.This process provides a new method for the protection of the acid sensitive hydroxyl group in 2 under mild condition.展开更多
文摘α-Oxoketene dithioacetals 2 via, 1,2-nucleophilic addition by allyl magnesium bromide afforded corresponding alcohols (3).Treated with water and catalyzed by Lewis acid, the alcohols 3 were converted regiospecifically to the conjugated 1,1—dialkylthio—1,3,5 hexatrienes (4). Both the alcohol 8 and its methoxy methyl ether 9 were sensative to dilute sulfuric acid and cyclized under this condition to form the aryl methylthio ether (10).
文摘α, α′ -Dioxo (ester ) ketene cyclic S, S-acetais 2 were reacted withethyleneddriine to chrd α, α′-dioxo (ester)ketene cyclic N, N-acetals 3 Thisprocess provides a new method for the synthesis of 3 in gnd yteld under mildcondition. All products are confirmed with elementai analpeis, IR, 1H NMR and13~C NMR
文摘Aliphatic α-oxo ketene cyclic dithioacetals 1 were reacted with allyl magne- sium bromide to afford the 1,2-addition products 2.Catalyzed by boron trifluoride etherate,the adducts 2 were etherified by methanol to afford the corresponding methyl ethers 3.This process provides a new method for the protection of the acid sensitive hydroxyl group in 2 under mild condition.
