Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2‑Substituted Cyclopentyl Aryl Ketones

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Main Authors: Zhengdong Ding, Feng Gao, Yining Lu, Qianjia Yuan, Wei-Ping Deng, Wanbin Zhang
Format: Article
Language:English
Published: American Chemical Society 2023-02-01
Series:Precision Chemistry
Online Access:https://doi.org/10.1021/prechem.2c00010
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author Zhengdong Ding
Feng Gao
Yining Lu
Qianjia Yuan
Wei-Ping Deng
Wanbin Zhang
author_facet Zhengdong Ding
Feng Gao
Yining Lu
Qianjia Yuan
Wei-Ping Deng
Wanbin Zhang
author_sort Zhengdong Ding
collection DOAJ
format Article
id doaj-art-d25b842e4d37442183bcd89c9953715f
institution OA Journals
issn 2771-9316
language English
publishDate 2023-02-01
publisher American Chemical Society
record_format Article
series Precision Chemistry
spelling doaj-art-d25b842e4d37442183bcd89c9953715f2025-08-20T02:26:04ZengAmerican Chemical SocietyPrecision Chemistry2771-93162023-02-011314615210.1021/prechem.2c00010Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2‑Substituted Cyclopentyl Aryl KetonesZhengdong Ding0Feng Gao1Yining Lu2Qianjia Yuan3Wei-Ping Deng4Wanbin Zhang5Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, ChinaShanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, ChinaShanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, ChinaShanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, ChinaShanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, Shanghai, ChinaShanghai Key Laboratory for Molecular Engineering of Chiral Drugs, Frontiers Science Center for Transformative Molecules, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, Chinahttps://doi.org/10.1021/prechem.2c00010
spellingShingle Zhengdong Ding
Feng Gao
Yining Lu
Qianjia Yuan
Wei-Ping Deng
Wanbin Zhang
Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2‑Substituted Cyclopentyl Aryl Ketones
Precision Chemistry
title Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2‑Substituted Cyclopentyl Aryl Ketones
title_full Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2‑Substituted Cyclopentyl Aryl Ketones
title_fullStr Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2‑Substituted Cyclopentyl Aryl Ketones
title_full_unstemmed Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2‑Substituted Cyclopentyl Aryl Ketones
title_short Asymmetric Hydrogenation of Tetrasubstituted α,β-Unsaturated Ketones: Access to Chiral 2‑Substituted Cyclopentyl Aryl Ketones
title_sort asymmetric hydrogenation of tetrasubstituted α β unsaturated ketones access to chiral 2 substituted cyclopentyl aryl ketones
url https://doi.org/10.1021/prechem.2c00010
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AT fenggao asymmetrichydrogenationoftetrasubstitutedabunsaturatedketonesaccesstochiral2substitutedcyclopentylarylketones
AT yininglu asymmetrichydrogenationoftetrasubstitutedabunsaturatedketonesaccesstochiral2substitutedcyclopentylarylketones
AT qianjiayuan asymmetrichydrogenationoftetrasubstitutedabunsaturatedketonesaccesstochiral2substitutedcyclopentylarylketones
AT weipingdeng asymmetrichydrogenationoftetrasubstitutedabunsaturatedketonesaccesstochiral2substitutedcyclopentylarylketones
AT wanbinzhang asymmetrichydrogenationoftetrasubstitutedabunsaturatedketonesaccesstochiral2substitutedcyclopentylarylketones