首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >Stereoselective epoxidation of aziridin-2-acrylaldehydes and azirinols synthesized from epoxyaldehydes catalyzed by NHC catalyst
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Stereoselective epoxidation of aziridin-2-acrylaldehydes and azirinols synthesized from epoxyaldehydes catalyzed by NHC catalyst

机译:由NHC催化剂催化的环氧丙烯醛合成的氮素-2-丙烯酸和氮吲哚的立体选择性环氧化

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摘要

Chiral aziridine-epoxyaldehydes (d.r. up to 99:1) have been obtained from stereoselective epoxidation of aziridin-2-acrylaldehyde in the presence of proline-derivatived catalyst. The desired aziridine-epoxyaldehydes can give valuable azirinols via ring opening reaction catalyzed by NBC catalyst. These azirinol derivatives are good candidates for the synthesis of more functionalized structures.
机译:在脯氨酸衍生的催化剂存在下,已经从唑突-2-丙烯醛的立体选择性环氧化获得了手性阿氮丙啶-环氧醛(D.R.至99:1)。 所需的氮丙啶-环氧醛可以通过NBC催化剂催化的开环反应给出有价值的氮素醇。 这些氮素衍生物是合成更官能化结构的良好候选者。

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