Article in Chemical science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
0numbers the graph read from it
0cells of the map it votes in
4citing 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.
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
9 authors.
Bo DingEngineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), Hubei Key Lab on Organic and Polymeric OptoElectronic Materials, College of Chemistry and Molecular Sciences, TaiKang Center for Life and Medical Sciences, Wuhan University Wuhan 430072 China qhzhou@whu.edu.cn.
Qilin XueEngineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), Hubei Key Lab on Organic and Polymeric OptoElectronic Materials, College of Chemistry and Molecular Sciences, TaiKang Center for Life and Medical Sciences, Wuhan University Wuhan 430072 China qhzhou@whu.edu.cn.
Han WeiThe Institute for Advanced Studies, Wuhan University Wuhan 430072 China.
Jiangwei ChenEngineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), Hubei Key Lab on Organic and Polymeric OptoElectronic Materials, College of Chemistry and Molecular Sciences, TaiKang Center for Life and Medical Sciences, Wuhan University Wuhan 430072 China qhzhou@whu.edu.cn.
Ze-Shui LiuEngineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), Hubei Key Lab on Organic and Polymeric OptoElectronic Materials, College of Chemistry and Molecular Sciences, TaiKang Center for Life and Medical Sciences, Wuhan University Wuhan 430072 China qhzhou@whu.edu.cn.
Hong-Gang ChengEngineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), Hubei Key Lab on Organic and Polymeric OptoElectronic Materials, College of Chemistry and Molecular Sciences, TaiKang Center for Life and Medical Sciences, Wuhan University Wuhan 430072 China qhzhou@whu.edu.cn.ORCID https://orcid.org/0000-0001-9585-9093
Hengjiang CongEngineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), Hubei Key Lab on Organic and Polymeric OptoElectronic Materials, College of Chemistry and Molecular Sciences, TaiKang Center for Life and Medical Sciences, Wuhan University Wuhan 430072 China qhzhou@whu.edu.cn.ORCID https://orcid.org/0000-0002-9225-0095
Jianting TangKey Laboratory of Water Environment Evolution and Pollution Control in Three Gorges Reservoir, School of Environmental and Chemical Engineering, Chongqing Three Gorges University Chongqing 404100 China.
Qianghui ZhouEngineering Research Center of Organosilicon Compounds & Materials (Ministry of Education), Hubei Key Lab on Organic and Polymeric OptoElectronic Materials, College of Chemistry and Molecular Sciences, TaiKang Center for Life and Medical Sciences, Wuhan University Wuhan 430072 China qhzhou@whu.edu.cn.ORCID https://orcid.org/0000-0002-8125-0380
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itself
Abstract
An efficient protocol for the asymmetric synthesis of fluorenols has been developed through an enantioconvergent process enabled by Pd(ii)/chiral norbornene cooperative catalysis. This approach allows facile access to diverse functionalized chiral fluorenols with constantly excellent enantioselectivities, applying readily available racemic secondary
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.
Enantioconvergent synthesis of chiral fluorenols from racemic secondary alcohols · full record | OpenQuestion