Journal
ORGANIC LETTERS
Volume 14, Issue 12, Pages 3044-3047Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol3011198
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Funding
- Chinese NSF [2097209, 21172140]
- Shanghai Institutions of Higher Learning Shanghai Education Committee
- Shanghai Leading Academic Discipline Project [S30107, J50101]
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The present work highlights unprecedented Ni-catalyzed reductive coupling of unactivated alkyl iodides with aryl acid chlorides to efficiently generate alkyl aryl ketones under mild conditions.
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