Journal
ORGANIC LETTERS
Volume 16, Issue 9, Pages 2358-2361Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol500677v
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Funding
- NIH [GM-61591]
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A new enantioselective peroxidation of alpha,beta-unsaturated nitroalkenes was realized with an easily accessible acid-base bifunctional organic catalyst derived from cinchona alkaloids. This reaction provides unprecedented easy access to optically active chiral peroxides, as illustrated by the asymmetric synthesis of beta-peroxy nitro compounds.
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