Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/182256
Title: Enantioselective synthesis of chiral acyclic nitriles containing α-all-carbon quaternary stereocenters via synergistic palladium and phase-transfer catalysis
Authors: Guo, Cheng
Dong, Yufei
Wang, Yiyang
Du, Xuan
Ma, Runxia
Tan, Choon-Hong
Luan, Xinjun
Ren, Jingyun
Keywords: Chemistry
Issue Date: 2024
Source: Guo, C., Dong, Y., Wang, Y., Du, X., Ma, R., Tan, C., Luan, X. & Ren, J. (2024). Enantioselective synthesis of chiral acyclic nitriles containing α-all-carbon quaternary stereocenters via synergistic palladium and phase-transfer catalysis. ACS Catalysis, 14(24), 18841-18850. https://dx.doi.org/10.1021/acscatal.4c06364
Journal: ACS Catalysis 
Abstract: Herein, we present a practical strategy for the asymmetric synthesis of chiral acyclic nitriles featuring α-all-carbon quaternary stereocenters, utilizing synergistic palladium and phase-transfer catalysis from allyl 2-cyanoacetates under mild conditions. This approach offers an efficient and reliable method for the in situ generation of tertiary α-cyano carbanions through intramolecular palladium-catalyzed decarboxylative allylic alkylation. Additionally, it enables highly enantioselective control of simple nitriles via ion-pairing interactions with chiral phase-transfer catalysts. The synthetic utility of this method is further demonstrated by its scalability to gram-scale synthesis and its subsequent transformation into a variety of chiral functionalized compounds containing acyclic all-carbon quaternary stereocenters.
URI: https://hdl.handle.net/10356/182256
ISSN: 2155-5435
DOI: 10.1021/acscatal.4c06364
Schools: School of Chemistry, Chemical Engineering and Biotechnology 
Rights: © 2024 American Chemical Society. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:CCEB Journal Articles

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