Evidence map›Paper›PMID 37349291›Full record

ArticleNature communications2023

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

Congcong Yin, Ya-Fei Jiang, Fanping Huang, Cong-Qiao Xu, Yingmin Pan, Shuang Gao, Gen-Qiang Chen, Xiaobing Ding, Shao-Tao Bai, Qiwei Lang and 2 more

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Congcong Yin *Department of Chemistry, Academy for Advanced Interdisciplinary Studies and Shenzhen Grubbs Institute, Southern University of Science and Technology, Shenzhen, 518055, China.
Ya-Fei Jiang *Department of Chemistry and Guangdong Provincial Key Laboratory of Catalytic Chemistry, Southern University of Science and Technology, Shenzhen, 518055, China.
Fanping HuangDepartment of Chemistry, Academy for Advanced Interdisciplinary Studies and Shenzhen Grubbs Institute, Southern University of Science and Technology, Shenzhen, 518055, China.
Cong-Qiao XuDepartment of Chemistry and Guangdong Provincial Key Laboratory of Catalytic Chemistry, Southern University of Science and Technology, Shenzhen, 518055, China.ORCID http://orcid.org/0000-0003-4593-3288
Yingmin PanDepartment of Chemistry, Academy for Advanced Interdisciplinary Studies and Shenzhen Grubbs Institute, Southern University of Science and Technology, Shenzhen, 518055, China.
Shuang GaoDepartment of Chemistry, Academy for Advanced Interdisciplinary Studies and Shenzhen Grubbs Institute, Southern University of Science and Technology, Shenzhen, 518055, China.
Gen-Qiang ChenDepartment of Chemistry, Academy for Advanced Interdisciplinary Studies and Shenzhen Grubbs Institute, Southern University of Science and Technology, Shenzhen, 518055, China.ORCID http://orcid.org/0000-0003-2276-6800
Xiaobing DingShenzhen Catalys Technology Co., Ltd, Shenzhen, 518100, China.
Shao-Tao BaiDepartment of Chemistry, Academy for Advanced Interdisciplinary Studies and Shenzhen Grubbs Institute, Southern University of Science and Technology, Shenzhen, 518055, China. shaotaobai@szpt.edu.cn.ORCID http://orcid.org/0000-0002-8991-1710
Qiwei LangShenzhen Catalys Technology Co., Ltd, Shenzhen, 518100, China. qwlang@catalys.com.cn.ORCID http://orcid.org/0000-0002-5608-0164
Jun LiDepartment of Chemistry and Guangdong Provincial Key Laboratory of Catalytic Chemistry, Southern University of Science and Technology, Shenzhen, 518055, China. junli@tsinghua.edu.cn.
Xumu ZhangDepartment of Chemistry, Academy for Advanced Interdisciplinary Studies and Shenzhen Grubbs Institute, Southern University of Science and Technology, Shenzhen, 518055, China. zhangxm@sustech.edu.cn.ORCID http://orcid.org/0000-0001-5700-0608

Funding

National Natural Science Foundation of China (National Science Foundation of China) 21991113National Natural Science Foundation of China (National Science Foundation of China) 22038002, 22033005
6 · The paper itself

Abstract

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

Indexed as

KetonesNicotineBiocatalysisCatalysisHydrogenationKetonesNicotine

Identifiers

PMID37349291
PMCPMC10287737

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.