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RhCl3·3H2O‑Catalyzed Regioselective C(sp2)−H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters
DepartmentOSSO国家重点实验室
Kang Zhao1,2; Rongrong Du1,2; Bingyang Wang1; Jianhua Liu1; Chungu Xia1; Lei Yang1
The second department纳米催化课题组
2019-05-13
Source PublicationACS Catalysis
Issue9Pages:5545−5551
Abstract


 

If12.221
compositor第一作者单位
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/25556
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorLei Yang
Affiliation1.中国科学院兰州化学物理研究所
2.中国科学院大学
Corresponding Author AffilicationLanzhou Institute of Chemical Physics,Chinese Academy of Sciences
Recommended Citation
GB/T 7714
Kang Zhao,Rongrong Du,Bingyang Wang,等. RhCl3·3H2O‑Catalyzed Regioselective C(sp2)−H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters[J]. ACS Catalysis,2019(9):5545−5551.
APA Kang Zhao,Rongrong Du,Bingyang Wang,Jianhua Liu,Chungu Xia,&Lei Yang.(2019).RhCl3·3H2O‑Catalyzed Regioselective C(sp2)−H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters.ACS Catalysis(9),5545−5551.
MLA Kang Zhao,et al."RhCl3·3H2O‑Catalyzed Regioselective C(sp2)−H Alkoxycarbonylation: Efficient Synthesis of Indole- and Pyrrole-2-carboxylic Acid Esters".ACS Catalysis .9(2019):5545−5551.
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