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首页> 外文期刊>Canadian Journal of Chemistry >Photochemistry of 9-methylbicyclo[3.3.1]nonyl aryl ketones - A novel 1,5-disproportionation of 1,4-hydroxy biradicals and asymmetric induction using the solid-state ionic chiral auxiliary method
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Photochemistry of 9-methylbicyclo[3.3.1]nonyl aryl ketones - A novel 1,5-disproportionation of 1,4-hydroxy biradicals and asymmetric induction using the solid-state ionic chiral auxiliary method

机译:9-甲基双环[3.3.1]壬基芳基酮的光化学-1,4-羟基双自由基的新型1,5-歧化和使用固态离子手性辅助方法的不对称诱导

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摘要

A novel 1,5-disproportionation reaction has been discovered for 1,4-hydroxy biradicals derived from the photolysis of 9-methylbicyclo[3.3.1]nonyl phenyl ketones(1),which undergo mainly Yang cyclization both in solution and the solid state.By applying the solid-state ionic chiral auxiliary method of asymmetric synthesis to the Yang cyclization,enantiomeric excesses as high as 95% were achieved at high reaction conversions.The origin of the reaction selectivity is discussed with the help of X-ray crystallography.In addition,the solid-state photoreaction of ketone 1b was found to occur in a single crystal-to-single crystal fashion.
机译:9,甲基双环[3.3.1]壬基苯基酮(1)的光解反应中发现的1,4-羟基双自由基发生了新的1,5-歧化反应,该反应在溶液和固态下均主要发生杨环化通过将不对称合成的固态离子手性辅助方法应用于杨环化反应,在高反应转化率下对映体过量高达95%。借助X射线晶体学讨论了反应选择性的起源。另外,发现酮1b的固态光反应以单晶至单晶的方式发生。

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