Aziridination of cyclohex-2-en-1-ol and geraniol: comparison with epoxidation
- 1 January 1988
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 9,p. 624-625
- https://doi.org/10.1039/c39880000624
Abstract
Aziridination of cyclohex-2-en-1-ol with 3-acetoxyamino-2-ethylquinazolone (1) is highly stereoselective, and reaction with geraniol is highly regioselective for the allylic alcohol double bond; comparisons are made with the corresponding reactions of peracids.Keywords
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