试剂
化学
亚砜
溶剂
二甲基亚砜
组合化学
有机化学
作者
Christine M. M. Hendriks,Philip Lamers,Julien Engel,Carsten Bolm
标识
DOI:10.1002/adsc.201300766
摘要
Abstract Sulfoxides can directly be converted into N ‐cyanosulfilimines using a new Burgess‐type reagent. By applying this strategy with a related reagent variant, synthetically valuable N H‐sulfoximines have been prepared from sulfoxides via N ‐protected sulfilimines. The practical three‐step reaction sequence is generally high yielding and applicable to a wide range of substrates. The sulfoxide‐to‐sulfilimine conversion can also be performed under solvent‐reduced conditions in a ball mill. magnified image
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