首页> 外文期刊>The Journal of Organic Chemistry >Copper(II)-Bis(oxazoline) catalyzed asymmetric Diels-Alder reaction with alpha'-arylsulfonyl enones as dienophiles
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Copper(II)-Bis(oxazoline) catalyzed asymmetric Diels-Alder reaction with alpha'-arylsulfonyl enones as dienophiles

机译:铜(II)-双(恶唑啉)催化的不对称Diels-Alder反应与作为亲二烯体的α'-芳基磺酰基烯酮

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摘要

[GRAPHICS] alpha'-Arylsulfonyl enones are efficient bidentate dienophiles for the Cu(II)-bis(oxazoline) catalyzed enantioselective Diels-Alder reaction with a number of dienes, affording the corresponding products with good to high enantiomeric excesses. The resulting products can be alkylated and the sulfone removed, so alpha'-arylsulfonyl enones can be regarded as surrogates of simple monodentate enones, which are poor dienophiles with this catalytic system.
机译:[图]α'-芳基磺酰基烯酮是Cu(II)-双(恶唑啉)催化的对映选择性Diels-Alder反应与许多二烯的有效二齿亲二烯体,提供了对映体过量至高对映体过量的相应产物。可以将所得产物烷基化并除去砜,因此α'-芳基磺酰基烯酮可以被视为简单单齿烯酮的替代物,该单齿烯酮在该催化体系中是弱亲二烯体。

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