期刊
ORGANIC LETTERS
卷 16, 期 9, 页码 2358-2361出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol500677v
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-
资金
- NIH [GM-61591]
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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