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首页> 外文期刊>Chemistry: A European journal >Catalytic asymmetric michael reactions of α,β-unsaturated ketones with sulfonyl-containing nucleophiles: Chiral synthesis of (R)-muscone and (S)-celery ketone
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Catalytic asymmetric michael reactions of α,β-unsaturated ketones with sulfonyl-containing nucleophiles: Chiral synthesis of (R)-muscone and (S)-celery ketone

机译:α,β-不饱和酮与含磺酰基亲核试剂的催化不对称迈克尔反应:(R)-麝香酮和(S)-芹菜酮的手性合成

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摘要

An amine worth its salt: A highly enantioselective Michael addition reaction of α,β-unsaturated ketones with the sulfonyl-containing nucleophiles bis(phenylsulfonyl)methane and 1-(phenylsulfonyl)propan-2-one, catalyzed by a chiral primary amine salt, has been developed and gives excellent enantioselectivities (see scheme). The methodology has successfully demonstrated its synthetic utility in the chiral synthesis of (R)-muscone and (S)-celery ketone.
机译:值得盐的胺:手性伯胺盐催化的α,β-不饱和酮与含磺酰基的亲核试剂双(苯磺酰基)甲烷和1-(苯磺酰基)丙-2-酮的高度对映选择性迈克尔加成反应,已开发并具有出色的对映选择性(参见方案)。该方法已成功证明了其在(R)-麝香酮和(S)-芹菜酮的手性合成中的合成效用。

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