Abstract
An unprecedented reaction mode of cyanogen bromide has been discovered. Under basic conditions, cyanogen bromide acts as an equivalent of both Br + and CN- to convert enolizable ketones into the corresponding cyanoepoxides in good yields. This unique reaction mode provides new, one-pot access to densely substituted cyanoepoxides from easily available ketones (see scheme).
Original language | English (US) |
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Pages (from-to) | 2808-2810 |
Number of pages | 3 |
Journal | Angewandte Chemie - International Edition |
Volume | 50 |
Issue number | 12 |
DOIs | |
State | Published - Mar 14 2011 |
Externally published | Yes |
Keywords
- cascade reactions
- cyanoepoxides
- cyanogen bromide
- synthetic methods
ASJC Scopus subject areas
- Catalysis
- Chemistry(all)