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|Title:||Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex||Authors:||Deng, Gongtao
|Keywords:||Engineering::Chemical engineering::Biochemical engineering||Issue Date:||2018||Source:||Deng, G., Chen, J., Sun, W., Bian, K., Jiang, Y., & Loh, T.-P. (2018). Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex. Advanced Synthesis & Catalysis, 360(20), 3900-3905. doi:10.1002/adsc.201800823||Journal:||Advanced Synthesis & Catalysis||Abstract:||An efficient bioinspired deamination method of both natural and unnatural amino acid derivatives has been developed. This method provides easy access to a wide variety of useful α, β‐unsaturated carbonyl compounds. The reaction is realized with two transition metal catalysts (palladium and Nickel) in‐easy handling procedure. A possible reaction pathway is also proposed and the control experiments support the involvement of the palladium‐catalyzed inert sp3 C−H activation as one of the key steps.||URI:||https://hdl.handle.net/10356/143699||ISSN:||1615-4169||DOI:||10.1002/adsc.201800823||Rights:||© 2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved.||Fulltext Permission:||none||Fulltext Availability:||No Fulltext|
|Appears in Collections:||SPMS Journal Articles|
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