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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Main Authors: Deng, Gongtao, Chen, Jie, Sun, Wangbin, Bian, Kehan, Jiang, Yaojia, Loh, Teck-Peng
Other Authors: School of Physical and Mathematical Sciences
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/143699
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Institution: Nanyang Technological University
Language: English
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spelling 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.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Engineering::Chemical engineering::Biochemical engineering
Bioinspired Reactions
C-H Activation
spellingShingle 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
description 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.
author2 School of Physical and Mathematical Sciences
author_facet 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
publishDate 2020
url https://hdl.handle.net/10356/143699
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