期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 15, 期 6, 页码 1334-1337出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ob02714h
关键词
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资金
- National Natural Science Foundation of China [21572025, 21672028]
- Key University Science Research Project of the Jiangsu Province [15KJA150001]
- Jiangsu Key Laboratory of Advanced Catalytic Materials Technology [BM2012110]
A palladium-catalyzed annulation of ortho-vinylanilines with dimethyl sulfoxide was developed to access 4-aryl quinolines in moderate to good yields. Activated by 1,4-diazabicyclo[2.2.2] octane bis(sulfur dioxide) adduct (DABSO), DMSO served as a =CH- fragment in this transformation. It represents a facile pathway leading to 4-aryl quinolines.
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