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Zhu, Zhixi, Hu, Qinru, Fu, Yi, Tong, Yingjia, Zhou, Zhi (2024) Design and Evolution of an Enzyme for the Asymmetric Michael Addition of Cyclic Ketones to Nitroolefins by Enamine Catalysis. Angewandte Chemie International Edition, 63 (33) doi:10.1002/anie.202404312

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Reference TypeJournal (article/letter/editorial)
TitleDesign and Evolution of an Enzyme for the Asymmetric Michael Addition of Cyclic Ketones to Nitroolefins by Enamine Catalysis
JournalAngewandte Chemie International Edition
AuthorsZhu, ZhixiAuthor
Hu, QinruAuthor
Fu, YiAuthor
Tong, YingjiaAuthor
Zhou, ZhiAuthor
Year2024 (August 12)Volume63
Issue33
PublisherWiley
DOIdoi:10.1002/anie.202404312Search in ResearchGate
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Mindat Ref. ID17543226Long-form Identifiermindat:1:5:17543226:6
GUID0
Full ReferenceZhu, Zhixi, Hu, Qinru, Fu, Yi, Tong, Yingjia, Zhou, Zhi (2024) Design and Evolution of an Enzyme for the Asymmetric Michael Addition of Cyclic Ketones to Nitroolefins by Enamine Catalysis. Angewandte Chemie International Edition, 63 (33) doi:10.1002/anie.202404312
Plain TextZhu, Zhixi, Hu, Qinru, Fu, Yi, Tong, Yingjia, Zhou, Zhi (2024) Design and Evolution of an Enzyme for the Asymmetric Michael Addition of Cyclic Ketones to Nitroolefins by Enamine Catalysis. Angewandte Chemie International Edition, 63 (33) doi:10.1002/anie.202404312
In(2024, August) Angewandte Chemie International Edition Vol. 63 (33) Wiley

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Zhu, Zhixi, Hu, Qinru, Fu, Yi, Tong, Yingjia, Zhou, Zhi (2024) Design and Evolution of an Enzyme for the Asymmetric Michael Addition of Cyclic Ketones to Nitroolefins by Enamine Catalysis. Angewandte Chemie, 136 (33) doi:10.1002/ange.202404312
Zhu, Zhixi, Hu, Qinru, Fu, Yi, Tong, Yingjia, Zhou, Zhi (2024) Frontispiece: Design and Evolution of an Enzyme for the Asymmetric Michael Addition of Cyclic Ketones to Nitroolefins by Enamine Catalysis. Angewandte Chemie International Edition, 63 (33) doi:10.1002/anie.202483362
Zhu, Zhixi, Hu, Qinru, Fu, Yi, Tong, Yingjia, Zhou, Zhi (2024) Frontispiz: Design and Evolution of an Enzyme for the Asymmetric Michael Addition of Cyclic Ketones to Nitroolefins by Enamine Catalysis. Angewandte Chemie, 136 (33) doi:10.1002/ange.202483362
Pan, Zhi‐Zhou, Li, Jia‐Heng, Tian, Hu, Yin, Liang (2024) Copper(I)‐Catalyzed Asymmetric Allylation of Ketones with 2‐Aza‐1,4‐Dienes. Angewandte Chemie International Edition, 63 (1) doi:10.1002/anie.202315293
Yu, Ming‐Zhu, Yuan, Ye, Li, Zhen‐Jie, Kunthic, Thittaya, Wang, He‐Xiang, Xu, Chen, Xiang, Zheng (2024) An Artificial Enzyme for Asymmetric Nitrocyclopropanation of α,β‐Unsaturated Aldehydes—Design and Evolution. Angewandte Chemie International Edition, 63 (25) doi:10.1002/anie.202401635
Shevchenko, Grigory A., Oppelaar, Barry, List, Benjamin (2018) An Unexpected α‐Oxidation of Cyclic Ketones with 1,4‐Benzoquinone by Enol Catalysis. Angewandte Chemie International Edition, 57 (33). 10756-10759 doi:10.1002/anie.201804445
Hu, Qinru; Feng, Liangyu; You, Ran; Zhu, Zhixi; Lei, Jie; Zhou, Zhi (2025) Design and Evolution of an Artificial Aldolase with an Abiological Catalytic Cofactor in Apo-Myoglobin. Organic Letters, 27 (37). doi:10.1021/acs.orglett.5c03309
Mechler, Melanie, Peters, René (2015) Diastereodivergent Asymmetric 1,4-Addition of Oxindoles to Nitroolefins by Using Polyfunctional Nickel-Hydrogen-Bond-Azolium Catalysts. Angewandte Chemie International Edition, 54 (35). 10303-10307 doi:10.1002/anie.201502930
Chen, Dian-Feng, Zhao, Feng, Hu, Yue, Gong, Liu-Zhu (2014) CH Functionalization/Asymmetric Michael Addition Cascade Enabled by Relay Catalysis: Metal Carbenoid Used for CC Bond Formation. Angewandte Chemie International Edition, 53 (40). 10763-10767 doi:10.1002/anie.201406098
Xu, Zhenghu, Liu, Lu, Wheeler, Kraig, Wang, Hong (2011) Asymmetric Inverse-Electron-Demand Hetero-Diels-Alder Reaction of Six-membered Cyclic Ketones: An Enamine/Metal Lewis Acid Bifunctional Approach. Angewandte Chemie International Edition, 50 (15). 3484-3488 doi:10.1002/anie.201100160
(2024) Corrigendum: Copper(I)‐Catalyzed Asymmetric Allylation of Ketones with 2‐Aza‐1,4‐Dienes. Angewandte Chemie International Edition, 63 (13) doi:10.1002/anie.202319011
 
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