Achiral organoiodine-functionalized helical polyisocyanides for multiple asymmetric dearomative oxidations

被引:31
作者
Wu, Zong-Quan [1 ]
Song, Xue [2 ]
Li, Yan-Xiang [2 ]
Zhou, Li [2 ]
Zhu, Yuan-Yuan [2 ]
Chen, Zheng [1 ]
Liu, Na [3 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Jilin, Peoples R China
[2] Hefei Univ Technol, Sch Chem & Chem Engn, Dept Polymer Sci & Engn, Hefei 230009, Peoples R China
[3] Jilin Univ, Sch Pharmaceut Sci, 1266 Fujin Road, Changchun 130021, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
LIVING POLYMERIZATION; POLYMERS; CATALYST; ENANTIOSELECTIVITY; SPIROLACTONIZATION; AMPLIFICATION; LIGANDS; AIR;
D O I
10.1038/s41467-023-36327-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Immobilizing organocatalyst onto helical polymers not only facilitates the catalyst recycling from homogeneous reactions, but also boosts enantioselectivity. In this work, achiral organoiodine-functionalized single left- and right-handed helical polyisocyanides were prepared from the same monomers, which catalyzed three asymmetric oxidations gave the desired products in high yields and excellent enantioselectivity. The enantiomeric excess of the target products was up to 95%. Remarkably, the enantioselectivity can be switched by reversing the helicity of the polymer backbone. The polymer catalysts can be facilely recovered and recycled in different asymmetric oxidations with maintained excellent activity and enantioselectivity. Immobilizing organocatalysts onto helical polymers can facilitate catalyst recycling and boost enantioselectivity. Here, the authors prepare achiral organoiodine-functionalized single left- and right-handed helical polyisocyanides from the same monomers and demonstrate their use in three asymmetric oxidations.
引用
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页数:11
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