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A 13-million turnover-number anionic Ir-catalyst for a selective industrial route to chiral nicotine

Developing catalysts with both useful enantioselectivities and million turnover numbers (TONs) for asymmetric hydrogenation of ketones is attractive for industrial production of high-value bioactive chiral entities but remains a challenging. Herein, we report an ultra-efficient anionic Ir-catalyst i...

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Autores principales: Yin, Congcong, Jiang, Ya-Fei, Huang, Fanping, Xu, Cong-Qiao, Pan, Yingmin, Gao, Shuang, Chen, Gen-Qiang, Ding, Xiaobing, Bai, Shao-Tao, Lang, Qiwei, Li, Jun, Zhang, Xumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287737/
https://www.ncbi.nlm.nih.gov/pubmed/37349291
http://dx.doi.org/10.1038/s41467-023-39375-8
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author Yin, Congcong
Jiang, Ya-Fei
Huang, Fanping
Xu, Cong-Qiao
Pan, Yingmin
Gao, Shuang
Chen, Gen-Qiang
Ding, Xiaobing
Bai, Shao-Tao
Lang, Qiwei
Li, Jun
Zhang, Xumu
author_facet Yin, Congcong
Jiang, Ya-Fei
Huang, Fanping
Xu, Cong-Qiao
Pan, Yingmin
Gao, Shuang
Chen, Gen-Qiang
Ding, Xiaobing
Bai, Shao-Tao
Lang, Qiwei
Li, Jun
Zhang, Xumu
author_sort Yin, Congcong
collection PubMed
description Developing catalysts with both useful enantioselectivities and million turnover numbers (TONs) for asymmetric hydrogenation of ketones is attractive for industrial production of high-value bioactive chiral entities but remains a challenging. Herein, we report an ultra-efficient anionic Ir-catalyst integrated with the concept of multidentate ligation for asymmetric hydrogenation of ketones. Biocatalysis-like efficacy of up to 99% ee (enantiomeric excess), 13,425,000 TON (turnover number) and 224 s(−1) TOF (turnover frequency) were documented for benchmark acetophenone. Up to 1,000,000 TON and 99% ee were achieved for challenging pyridyl alkyl ketone where at most 10,000 TONs are previously reported. The anionic Ir-catalyst showed a novel preferred ONa/MH instead of NNa/MH bifunctional mechanism. A selective industrial route to enantiopure nicotine has been established using this anionic Ir-catalyst for the key asymmetric hydrogenation step at 500 kg batch scale, providing 40 tons scale of product.
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spelling pubmed-102877372023-06-24 A 13-million turnover-number anionic Ir-catalyst for a selective industrial route to chiral nicotine Yin, Congcong Jiang, Ya-Fei Huang, Fanping Xu, Cong-Qiao Pan, Yingmin Gao, Shuang Chen, Gen-Qiang Ding, Xiaobing Bai, Shao-Tao Lang, Qiwei Li, Jun Zhang, Xumu Nat Commun Article Developing catalysts with both useful enantioselectivities and million turnover numbers (TONs) for asymmetric hydrogenation of ketones is attractive for industrial production of high-value bioactive chiral entities but remains a challenging. Herein, we report an ultra-efficient anionic Ir-catalyst integrated with the concept of multidentate ligation for asymmetric hydrogenation of ketones. Biocatalysis-like efficacy of up to 99% ee (enantiomeric excess), 13,425,000 TON (turnover number) and 224 s(−1) TOF (turnover frequency) were documented for benchmark acetophenone. Up to 1,000,000 TON and 99% ee were achieved for challenging pyridyl alkyl ketone where at most 10,000 TONs are previously reported. The anionic Ir-catalyst showed a novel preferred ONa/MH instead of NNa/MH bifunctional mechanism. A selective industrial route to enantiopure nicotine has been established using this anionic Ir-catalyst for the key asymmetric hydrogenation step at 500 kg batch scale, providing 40 tons scale of product. Nature Publishing Group UK 2023-06-22 /pmc/articles/PMC10287737/ /pubmed/37349291 http://dx.doi.org/10.1038/s41467-023-39375-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yin, Congcong
Jiang, Ya-Fei
Huang, Fanping
Xu, Cong-Qiao
Pan, Yingmin
Gao, Shuang
Chen, Gen-Qiang
Ding, Xiaobing
Bai, Shao-Tao
Lang, Qiwei
Li, Jun
Zhang, Xumu
A 13-million turnover-number anionic Ir-catalyst for a selective industrial route to chiral nicotine
title A 13-million turnover-number anionic Ir-catalyst for a selective industrial route to chiral nicotine
title_full A 13-million turnover-number anionic Ir-catalyst for a selective industrial route to chiral nicotine
title_fullStr A 13-million turnover-number anionic Ir-catalyst for a selective industrial route to chiral nicotine
title_full_unstemmed A 13-million turnover-number anionic Ir-catalyst for a selective industrial route to chiral nicotine
title_short A 13-million turnover-number anionic Ir-catalyst for a selective industrial route to chiral nicotine
title_sort 13-million turnover-number anionic ir-catalyst for a selective industrial route to chiral nicotine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10287737/
https://www.ncbi.nlm.nih.gov/pubmed/37349291
http://dx.doi.org/10.1038/s41467-023-39375-8
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