A redox-neutral catechol synthesis
Catechols are common structural motifs in bioactive molecules and synthetic building blocks. Here the authors report a method to convert phenol derivatives into catechols via an iridium-catalysed redox-neutral C–H hydroxylation, giving diversely substituted products under mild conditions.
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2017-01-01
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Online Access: | https://doi.org/10.1038/ncomms14227 |
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doaj-928132b5484e4544bc685b1aa58106ca2021-05-11T07:34:30ZengNature Publishing GroupNature Communications2041-17232017-01-01811910.1038/ncomms14227A redox-neutral catechol synthesisQian Wu0Dingyuan Yan1Ying Chen2Ting Wang3Feng Xiong4Wei Wei5Yi Lu6Wei-Yin Sun7Jie Jack Li8Jing Zhao9Guangdong Key Lab of Nano-Micro Material Research, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate SchoolDepartment of Chemistry, State Key Laboratory of Coordination Chemistry, Institute of Chemistry and BioMedical Sciences, School of Chemistry and Chemical Engineering, Collaborative Innovation Centre of Chemistry for Life Sciences, Nanjing UniversityGuangdong Key Lab of Nano-Micro Material Research, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate SchoolSchool of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate SchoolDepartment of Chemistry, State Key Laboratory of Coordination Chemistry, Institute of Chemistry and BioMedical Sciences, School of Chemistry and Chemical Engineering, Collaborative Innovation Centre of Chemistry for Life Sciences, Nanjing UniversityDepartment of Chemistry, State Key Laboratory of Coordination Chemistry, Institute of Chemistry and BioMedical Sciences, School of Chemistry and Chemical Engineering, Collaborative Innovation Centre of Chemistry for Life Sciences, Nanjing UniversityDepartment of Chemistry, State Key Laboratory of Coordination Chemistry, Institute of Chemistry and BioMedical Sciences, School of Chemistry and Chemical Engineering, Collaborative Innovation Centre of Chemistry for Life Sciences, Nanjing UniversityDepartment of Chemistry, State Key Laboratory of Coordination Chemistry, Institute of Chemistry and BioMedical Sciences, School of Chemistry and Chemical Engineering, Collaborative Innovation Centre of Chemistry for Life Sciences, Nanjing UniversityDepartment of Chemistry, University of San FranciscoGuangdong Key Lab of Nano-Micro Material Research, School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate SchoolCatechols are common structural motifs in bioactive molecules and synthetic building blocks. Here the authors report a method to convert phenol derivatives into catechols via an iridium-catalysed redox-neutral C–H hydroxylation, giving diversely substituted products under mild conditions.https://doi.org/10.1038/ncomms14227 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Qian Wu Dingyuan Yan Ying Chen Ting Wang Feng Xiong Wei Wei Yi Lu Wei-Yin Sun Jie Jack Li Jing Zhao |
spellingShingle |
Qian Wu Dingyuan Yan Ying Chen Ting Wang Feng Xiong Wei Wei Yi Lu Wei-Yin Sun Jie Jack Li Jing Zhao A redox-neutral catechol synthesis Nature Communications |
author_facet |
Qian Wu Dingyuan Yan Ying Chen Ting Wang Feng Xiong Wei Wei Yi Lu Wei-Yin Sun Jie Jack Li Jing Zhao |
author_sort |
Qian Wu |
title |
A redox-neutral catechol synthesis |
title_short |
A redox-neutral catechol synthesis |
title_full |
A redox-neutral catechol synthesis |
title_fullStr |
A redox-neutral catechol synthesis |
title_full_unstemmed |
A redox-neutral catechol synthesis |
title_sort |
redox-neutral catechol synthesis |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2017-01-01 |
description |
Catechols are common structural motifs in bioactive molecules and synthetic building blocks. Here the authors report a method to convert phenol derivatives into catechols via an iridium-catalysed redox-neutral C–H hydroxylation, giving diversely substituted products under mild conditions. |
url |
https://doi.org/10.1038/ncomms14227 |
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