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DOI10.1073/pnas.2109408118
Electrochemical borylation of carboxylic acids
Barton L.M.; Chen L.; Blackmond D.G.; Baran P.S.
发表日期2021
ISSN0027-8424
卷号118期号:34
英文摘要A simple electrochemically mediated method for the conversion of alkyl carboxylic acids to their borylated congeners is presented. This protocol features an undivided cell setup with inexpensive carbon-based electrodes and exhibits a broad substrate scope and scalability in both flow and batch reactors. The use of this method in challenging contexts is exemplified with a modular formal synthesis of jawsamycin, a natural product harboring five cyclopropane rings. © 2021 National Academy of Sciences. All rights reserved.
英文关键词Electrochemistry; Organic synthesis; Total synthesis
语种英语
来源期刊Proceedings of the National Academy of Sciences of the United States of America
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/238420
作者单位Department of Chemistry, Scripps Research, San Diego, CA 92037, United States
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Barton L.M.,Chen L.,Blackmond D.G.,et al. Electrochemical borylation of carboxylic acids[J],2021,118(34).
APA Barton L.M.,Chen L.,Blackmond D.G.,&Baran P.S..(2021).Electrochemical borylation of carboxylic acids.Proceedings of the National Academy of Sciences of the United States of America,118(34).
MLA Barton L.M.,et al."Electrochemical borylation of carboxylic acids".Proceedings of the National Academy of Sciences of the United States of America 118.34(2021).
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