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首页> 外文期刊>Chemistry: A European journal >Organocatalytic enantioselective amination of Morita-Baylis-Hillman carbonates with masked ammonia: A facile method for the synthesis of unprotected α-methylene-β-amino esters
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Organocatalytic enantioselective amination of Morita-Baylis-Hillman carbonates with masked ammonia: A facile method for the synthesis of unprotected α-methylene-β-amino esters

机译:含屏蔽氨的Morita-Baylis-Hillman碳酸盐的有机催化对映选择性胺化:合成未保护的α-亚甲基-β-氨基酯的简便方法

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摘要

Amination under the mask: The asymmetric allylic amination of MBH carbonates was achieved with masked ammonia (benzophenone imine) under the catalysis of modified cinchona alkaloids to give good yields with excellent enantioselectivities (up to 99% ee) for a wide range of MBH carbonates (see scheme).
机译:掩膜下的胺化:在改性金鸡纳生物碱的催化下,用掩蔽的氨(二苯甲酮亚胺)实现了MBH碳酸酯的不对称烯丙基胺化,从而获得了良好的收率,并具有出色的对映选择性(高达99%ee),适用于多种MBH碳酸酯(参见方案)。

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