首页> 外文期刊>The Journal of Organic Chemistry >Diastereoselective Synthesis of N-Secondary Alkyl 2-Alkoxymethylpyrrolidines via Sequential Addition Reactions of Organolithium and -Magnesium Reagents to N-Thioformyl 2-Alkoxymethylpyrrolidines
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Diastereoselective Synthesis of N-Secondary Alkyl 2-Alkoxymethylpyrrolidines via Sequential Addition Reactions of Organolithium and -Magnesium Reagents to N-Thioformyl 2-Alkoxymethylpyrrolidines

机译:通过有机锂和镁试剂与N-硫甲酰基2-烷氧基甲基吡咯烷酮的顺序加成反应,非对映选择性地合成N-仲烷基2-烷氧基甲基吡咯烷酮

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摘要

Highly efficient sequential addition reactions of organolithium and -magnesium reagents to N-thioformyl 2-methoxymethylpyrrolidine have been described. Various combinations of these reagents gives successful results. A highly efficient and diastereoselective addition reaction is also described. Use of the opposite combinations of substituents on organolithium and -magnesium reagents leads to the selective formation of the opposite diastereomers. The reaction was extended to N-thioformyl 2-siloxymethypyrrolidine and 2-methoxymethylpiperidine, and these showed similar efficiency and selectivity.
机译:已经描述了有机锂和-镁试剂与N-硫代甲酰基2-甲氧基甲基吡咯烷的高效顺序加成反应。这些试剂的各种组合可产生成功的结果。还描述了高效和非对映选择性加成反应。在有机锂和镁试剂上使用相反的取代基组合会导致相反的非对映异构体的选择性形成。反应扩展到N-硫代甲酰基2-甲硅烷氧基甲基吡咯烷和2-甲氧基甲基哌啶,它们显示出相似的效率和选择性。

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