Journal
ORGANIC LETTERS
Volume 18, Issue 23, Pages 6082-6085Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.6b03069
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Funding
- University of Nevada, Reno
- ACS-PRF award [DNI-51442]
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The novel reactivity of in situ generated azaoxyally1 cation intermediates with a variety of carbonyl compounds is reported to construct 4-oxazolidinones motifs with good yields and diastereoselectivities. This simple and efficient (3 + 2) cycloaddition method provides direct access to potential bioactive compounds.
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