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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Diastereoselective Baylis–Hillman reaction using N-glyoxyloyl camphorpyrazolidinone as an electrophile: synthesis of optically pure 2-hydroxy-3-methylene succinic acid derivative
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Diastereoselective Baylis–Hillman reaction using N-glyoxyloyl camphorpyrazolidinone as an electrophile: synthesis of optically pure 2-hydroxy-3-methylene succinic acid derivative

机译:非对映选择性Baylis-Hillman反应,使用N-乙氧基酰樟脑吡唑烷二酮作为亲电试剂:光学纯的2-羟基-3-亚甲基琥珀酸衍生物的合成

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摘要

The camphorpyrazolidinone derived N-glyoxylate was efficiently prepared and used as an electrophile in the Baylis–Hillman reaction under classical DABCO catalyzed conditions. The corresponding 2-hydroxy-3-methylene succinic acid derivative was generally obtained with excellent diastereoselectivity and moderate chemical yields (51–75%).
机译:有效地制备了由樟脑吡唑烷酮衍生的N-乙醛酸酯,并在经典DABCO催化条件下将其用作亲电子试剂用于Baylis-Hillman反应。通常获得的2-羟基-3-亚甲基琥珀酸衍生物具有出色的非对映选择性和中等化学收率(51-75%)。

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