Access to P-stereogenic compounds via desymmetrizing enantioselective bromination.

Access to P-stereogenic compounds via desymmetrizing enantioselective bromination.
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通过对映选择性溴化的对称对映选择性溴化,可以访问P-肌发育化合物。

DOI:
10.1039/d0sc07008d
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发表时间:
2021-02-12
期刊:
影响因子:
8.4
通讯作者:
Li X
Li X
中科院分区:
化学1区
文献类型:
--
作者:
Huang QH;Zhou QY;Yang C;Chen L;Cheng JP;Li X

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A novel and efficient desymmetrizing asymmetric ortho-selective mono-bromination of bisphenol phosphine oxides under chiral squaramide catalysis was reported. Using this asymmetric ortho-bromination strategy, a wide range of chiral bisphenol phosphine oxides and bisphenol phosphinates were obtained with good to excellent yields (up to 92%) and enantioselectivities (up to 98.5 : 1.5 e.r.). The reaction could be scaled up, and the synthetic utility of the desired P-stereogenic compounds was proved by transformations and application in an asymmetric reaction. A highly efficient desymmetrizing asymmetric bromination of bisphenol phosphine oxides was developed, providing a wide range of chiral bisphenol phosphine oxides and bisphenol phosphinates with high yields and enantioselectivities.
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