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D155850-100mlCyclohexanone dimethyl ketal reacts with trimethylsilane in the presence of trimethylsilyl triflate to form the corresponding ether. It can also undergo allylation and propargylation in the presence of indium to form the corresponding homoallylic or
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D155850-25mlCyclohexanone dimethyl ketal reacts with trimethylsilane in the presence of trimethylsilyl triflate to form the corresponding ether. It can also undergo allylation and propargylation in the presence of indium to form the corresponding homoallylic or
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D155850-5mlCyclohexanone dimethyl ketal reacts with trimethylsilane in the presence of trimethylsilyl triflate to form the corresponding ether. It can also undergo allylation and propargylation in the presence of indium to form the corresponding homoallylic or
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D155928-1ml1,1-Dimethoxycyclopentane.
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D155928-5ml1,1-Dimethoxycyclopentane.
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D472280-1g1,1-Dimethoxyhexane.
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D472280-25g1,1-Dimethoxyhexane.
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D472280-5g1,1-Dimethoxyhexane.
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D154660-100g1,1-Dimethylguanidine sulfate salt has been employed: . as peroxide activator for bleaching cellulosic textiles . in the synthesis of N2,N2-dimethyl-4-(1-methyl-1H-indol-3-yl)pyrimidine-2,5-diamine, substrate for the modified Pictet-Spengler
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D154660-1g1,1-Dimethylguanidine sulfate salt has been employed: . as peroxide activator for bleaching cellulosic textiles . in the synthesis of N2,N2-dimethyl-4-(1-methyl-1H-indol-3-yl)pyrimidine-2,5-diamine, substrate for the modified Pictet-Spengler
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D154660-25g1,1-Dimethylguanidine sulfate salt has been employed: . as peroxide activator for bleaching cellulosic textiles . in the synthesis of N2,N2-dimethyl-4-(1-methyl-1H-indol-3-yl)pyrimidine-2,5-diamine, substrate for the modified Pictet-Spengler
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D154660-500g1,1-Dimethylguanidine sulfate salt has been employed: . as peroxide activator for bleaching cellulosic textiles . in the synthesis of N2,N2-dimethyl-4-(1-methyl-1H-indol-3-yl)pyrimidine-2,5-diamine, substrate for the modified Pictet-Spengler