Highly Diastereoselective Synthesis of 2,2-Disubstituted Cyclopentane-1,3-diols via Stepwise Ketone Reduction Enabling Concise Chirality Construction.

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第一作者： Jingyao,Gong

第一单位： Department of Medicinal Chemistry, School of Pharmacy, Southwest Medical University, Luzhou, Sichuan 646000, China.

作者： Jingyao,Gong ^[1] ; Jianjiong,Li ^[2] ; Xi,Chen ^[2] ; Hongliu,Zhang ^[2] ; Liangyan,Zhu ^[2] ; Dandan,Bu ^[2] ; Qin,Wang ^[2] ; Jinhui,Feng ^[1] ; Qiaqing,Wu ^[2] ; Dunming,Zhu ^[2]

作者单位： Department of Medicinal Chemistry, School of Pharmacy, Southwest Medical University, Luzhou, Sichuan 646000, China. ^[1] National Engineering Laboratory for Industrial Enzymes and Tianjin Engineering Research Center of Biocatalytic Technology, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, 32 West seventh Avenue, Tianjin Airport Economic Area, Tianjin 300308, China. ^[2]

DOI 10.1021/acs.joc.0c00851

PMID 32668161

发布时间 2021-01-27

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The Journal of organic chemistry

2020年85卷15期

9599-9606页

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Highly Diastereoselective Synthesis of 2,2-Disubstituted Cyclopentane-1,3-diols via Stepwise Ketone Reduction Enabling Concise Chirality Construction.

The Journal of organic chemistry

相似文献

The Journal of organic chemistry

相关期刊

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Highly Diastereoselective Synthesis of 2,2-Disubstituted Cyclopentane-1,3-diols via Stepwise Ketone Reduction Enabling Concise Chirality Construction.

The Journal of organic chemistry

相似文献

The Journal of organic chemistry

相关期刊

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