Catalyst-free C-N bond formation under biocompatible reaction conditions
A C-N bond formation reaction under biocompatible conditions for the amination of allenic ketone compounds to access a diversity of β-keto enamines is developed. This reaction is atom economical, green, and highly regioselective and works well with many structurally important amines such as amino su...
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sg-ntu-dr.10356-1622302023-02-28T20:09:08Z Catalyst-free C-N bond formation under biocompatible reaction conditions Goh, Jeffrey Ong, Seng Kheong Tan, Yan Sheng Loh, Teck-Peng School of Physical and Mathematical Sciences Science::Chemistry Amino Acid Esters Bond Formation A C-N bond formation reaction under biocompatible conditions for the amination of allenic ketone compounds to access a diversity of β-keto enamines is developed. This reaction is atom economical, green, and highly regioselective and works well with many structurally important amines such as amino sugar and amino acid esters or peptides. A wide array of β-keto enamines was obtained in modest to excellent yields with wide functional group tolerance using this protocol. A gram-scale synthesis of an anti-microbial agent was also realized using this strategy under green reaction conditions. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Nanyang Technological University Published version The authors gratefully acknowledge the financial support from the Distinguished University Professor grant (Nanyang Technological University, Singapore), AcRF Tier 1 grants from the Ministry of Education of Singapore (RG107/19, RG11/20 and RT14/20), and the Agency for Science, Technology and Research (A*Star) under its MTC Individual Research Grant (IRG). 2022-10-10T07:50:32Z 2022-10-10T07:50:32Z 2022 Journal Article Goh, J., Ong, S. K., Tan, Y. S. & Loh, T. (2022). Catalyst-free C-N bond formation under biocompatible reaction conditions. Green Chemistry, 24(8), 3321-3325. https://dx.doi.org/10.1039/d2gc00027j 1463-9262 https://hdl.handle.net/10356/162230 10.1039/d2gc00027j 2-s2.0-85129284897 8 24 3321 3325 en RG107/19 RG11/20 RT14/20 Green Chemistry © 2022 The Royal Society of Chemistry. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. application/pdf |
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Science::Chemistry Amino Acid Esters Bond Formation Goh, Jeffrey Ong, Seng Kheong Tan, Yan Sheng Loh, Teck-Peng Catalyst-free C-N bond formation under biocompatible reaction conditions |
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A C-N bond formation reaction under biocompatible conditions for the amination of allenic ketone compounds to access a diversity of β-keto enamines is developed. This reaction is atom economical, green, and highly regioselective and works well with many structurally important amines such as amino sugar and amino acid esters or peptides. A wide array of β-keto enamines was obtained in modest to excellent yields with wide functional group tolerance using this protocol. A gram-scale synthesis of an anti-microbial agent was also realized using this strategy under green reaction conditions. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Goh, Jeffrey Ong, Seng Kheong Tan, Yan Sheng Loh, Teck-Peng |
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Article |
author |
Goh, Jeffrey Ong, Seng Kheong Tan, Yan Sheng Loh, Teck-Peng |
author_sort |
Goh, Jeffrey |
title |
Catalyst-free C-N bond formation under biocompatible reaction conditions |
title_short |
Catalyst-free C-N bond formation under biocompatible reaction conditions |
title_full |
Catalyst-free C-N bond formation under biocompatible reaction conditions |
title_fullStr |
Catalyst-free C-N bond formation under biocompatible reaction conditions |
title_full_unstemmed |
Catalyst-free C-N bond formation under biocompatible reaction conditions |
title_sort |
catalyst-free c-n bond formation under biocompatible reaction conditions |
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2022 |
url |
https://hdl.handle.net/10356/162230 |
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1759854062608580608 |