Journal
ORGANIC LETTERS
Volume 16, Issue 9, Pages 2498-2501Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol500869p
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Funding
- Fundamental Research Funds for the Central Universities [WK2060190022, WK2060190026]
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A strategy of ruthenium-catalyzed self-hydride transferring cleavage of N-O bonds was designed and utilized in a cascade 1,3-dipolar cyclization of alkenes and N-methyl nitrones followed by an N-demethylative rearrangement, furnishing synthetically useful N-H 1,3-oxazinanes.
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