Wei Xue
Guizhou University
6 Papers
12 Citations
Wei Xue is an academic researcher from Guizhou University. The author has contributed to research in topics: Carbene & Catalysis. The author has an hindex of 6, co-authored 6 publications.
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Papers
Carbene-Catalyzed Enantioselective Aromatic N-Nucleophilic Addition of Heteroarenes to Ketones
Yonggui Liu,Guoyong Luo,Xing Yang,Jiang Shichun,Wei Xue,Yonggui Robin Chi,Yonggui Robin Chi,Zhichao Jin +7 more
TL;DR: Several of the chiral N,O-acetal products afforded through this protocol exhibit excellent anti-bacterial activities against Rs and are valuable in the development of novel agrichemicals for plant protection.
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Carbene-Catalyzed α-Carbon Amination of Chloroaldehydes for Enantioselective Access to Dihydroquinoxaline Derivatives.
Ruoyan Huang,Xingkuan Chen,Chengli Mou,Guoyong Luo,Yongjia Li,Xiangyang Li,Wei Xue,Zhichao Jin,Yonggui Robin Chi,Yonggui Robin Chi +9 more
TL;DR: An NHC-catalyzed α-carbon amination of chloroaldehydes was developed that affords optically enriched dihydroquinoxalines that are core structures in natural products and synthetic bioactive molecules.
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Direct activation of β-sp3-carbons of saturated carboxylic esters as electrophilic carbons via oxidative carbene catalysis
Bin Liu,Weihong Wang,Ruoyan Huang,Jiekuan Yan,Jichang Wu,Wei Xue,Song Yang,Zhichao Jin,Yonggui Robin Chi,Yonggui Robin Chi +9 more
TL;DR: An N-heterocyclic carbene-catalyzed oxidative LUMO activation of the β-cabons of saturated carboxylic esters is disclosed and the use of HOBt as an additive was found to significantly improve both yields and enantioselectivities of the reactions.
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Efficient Access to 2‐Pyrones via Carbene‐Catalyzed Oxidative [3+3] Reactions between Enals and Nitrogen Ylides
Pengcheng Zheng,Chengcheng Li,Chengli Mou,Dingwu Pan,Shuquan Wu,Wei Xue,Zhichao Jin,Yonggui Robin Chi,Yonggui Robin Chi +8 more
TL;DR: In this paper, a carbene-catalyzed oxidative cycloaddition reaction between enals and nitrogen ylides was reported for quick access to 2-pyrones, which can be used as building blocks for the preparation of sophisticated functional molecules.
16
Addition of N-Heterocyclic Carbene Catalyst to Aryl Esters Induces Remote C-Si Bond Activation and Benzylic Carbon Functionalization.
Hongling Wang,Xingkuan Chen,Yongjia Li,Jilan Wang,Shuquan Wu,Wei Xue,Song Yang,Yonggui Robin Chi,Yonggui Robin Chi +8 more
TL;DR: Through the incorporation of a silicon atom to an aryl carboxylic ester substrate, the resulting C-Si bond can be activated via the addition of a carbene catalyst on a remote site, which allows for efficient functionalization of the benzylic sp3-carbons of aryL carboxYlic esters.