奎尼嗪
吲哚嗪
哌啶
化学
二羟基化
立体化学
有机化学
对映选择合成
生物碱
催化作用
作者
Barbara Bernardim,Leonardo D. Lordello,Antonio C. B. Burtoloso
标识
DOI:10.2174/15680266113139990145
摘要
A four-step approach for the synthesis of dihydroxylated piperidine, quinolizidine and indolizidine systems is described employing α,β-unsaturated diazoketones as versatile building blocks. Unsaturated diazoketones were readily prepared from a Horner-Wadsworth-Emmons reaction between a diazophosphonate and amino-aldehydes. The strategy employs an asymmetric dihydroxylation reaction as the key step and is simple and straightforward enough to be extended to other nitrogen heterocycles. Keywords: Diazocompounds, glucosidases, indolizidines, piperidines, quinolizidines, α, β-unsaturated diazoketones.
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