Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex
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) i...
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sg-ntu-dr.10356-1436992020-09-17T05:11:08Z Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex Deng, Gongtao Chen, Jie Sun, Wangbin Bian, Kehan Jiang, Yaojia Loh, Teck-Peng School of Physical and Mathematical Sciences Engineering::Chemical engineering::Biochemical engineering Bioinspired Reactions C-H Activation 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. 2020-09-17T05:11:08Z 2020-09-17T05:11:08Z 2018 Journal Article 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 1615-4169 https://hdl.handle.net/10356/143699 10.1002/adsc.201800823 20 360 3900 3905 en Advanced Synthesis & Catalysis © 2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim. All rights reserved. |
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Engineering::Chemical engineering::Biochemical engineering Bioinspired Reactions C-H Activation Deng, Gongtao Chen, Jie Sun, Wangbin Bian, Kehan Jiang, Yaojia Loh, Teck-Peng Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex |
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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. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Deng, Gongtao Chen, Jie Sun, Wangbin Bian, Kehan Jiang, Yaojia Loh, Teck-Peng |
format |
Article |
author |
Deng, Gongtao Chen, Jie Sun, Wangbin Bian, Kehan Jiang, Yaojia Loh, Teck-Peng |
author_sort |
Deng, Gongtao |
title |
Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex |
title_short |
Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex |
title_full |
Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex |
title_fullStr |
Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex |
title_full_unstemmed |
Bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex |
title_sort |
bioinspired deamination of α-amino acid derivatives catalyzed by a palladium/nickel complex |
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2020 |
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https://hdl.handle.net/10356/143699 |
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1681058070186164224 |