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首页> 外文期刊>Beilstein journal of organic chemistry. >Chiral multifunctional thiourea-phosphine catalyzed asymmetric [3 + 2] annulation of Morita–Baylis–Hillman carbonates with maleimides
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Chiral multifunctional thiourea-phosphine catalyzed asymmetric [3 + 2] annulation of Morita–Baylis–Hillman carbonates with maleimides

机译:手性多功能硫脲磷化氢催化森田-贝利斯-希尔曼碳酸盐与马来酰亚胺的不对称[3 + 2]环化

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摘要

We have developed a multifunctional thiourea-phosphine catalyzed asymmetric [3 + 2] annulation of Morita–Baylis–Hillman (MBH) carbonates with maleimides, which can efficiently construct functionalized cyclopentenes bearing three contiguous stereocenters in moderate to excellent yields and excellent diastereo- and enantioselectivities. A plausible mechanism has been also proposed on the basis of control experiments and previous literature.
机译:我们开发了一种多功能硫脲-膦催化的森田-贝利斯-希尔曼(MBH)碳酸盐与马来酰亚胺的不对称[3 + 2]环化反应,可以有效地构建具有三个连续立体中心的官能化环戊烯,并具有中等至优异的产率以及出色的非对映异构和对映选择性。在控制实验和以前的文献的基础上,也提出了一个合理的机制。

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