Total synthesis of chiral biaryl natural products by asymmetric biaryl coupling.

Total synthesis of chiral biaryl natural products by asymmetric biaryl coupling.
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DOI:
10.1039/b821092f
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发表时间:
2009-11
影响因子:
46.2
通讯作者:
Linton EC
Linton EC
中科院分区:
化学1区
文献类型:
--
作者:
Kozlowski MC;Morgan BJ;Linton EC

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本教程的审查强调使用催化不对称2-萘酚偶联全合成。概述了手性的类型、手性联芳基天然产物、手性联芳基天然产物的制备方法以及其它催化不对称联芳基偶联反应。介绍了2-萘酚偶联反应的三大类手性催化剂(Cu、V、Fe),并讨论了它们的局限性和优点。讨论了铜催化偶联在仿生合成中的应用,包括尼日利亚酮、竹红菌素、calphostin D、草色素和尾孢菌素。
This tutorial review highlights the use of catalytic asymmetric 2-naphthol couplings in total synthesis. The types of chirality, chiral biaryl natural products, prior approaches to chiral biaryl natural products, and other catalytic asymmetric biaryl couplings are outlined. The three main categories of chiral catalysts for 2-naphthol coupling (Cu, V, Fe) are described with discussion of their limitations and advantages. Applications of the copper catalyzed couplings in biomimetic syntheses are discussed including nigerone, hypocrellin, calphostin D, phleichrome, and cercosporin.
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