Journal
ORGANIC LETTERS
Volume 18, Issue 15, Pages 3702-3705Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b01740
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Funding
- National Natural Science Foundation of China [21202049]
- Recruitment Program of Global Experts (1000 Talents Plan)
- Natural Science Foundation of Fujian Province [2016J01064]
- Fujian Hundred Talents Plan and Program of Innovative Research Team of Huaqiao University [Z14X0047]
- Graduate Innovation Fund of Huaqiao University
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A novel domino palladium-catalyzed nitration of Meyer-Schuster intermediates which were generated in situ from propargylic alcohols was developed, by the use of t-BuONO, leading to alpha-nitro enones in good to excellent yields at room temperature with a broad functional group tolerance.
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