The direct electrophilic α-cyanation of β-keto esters and amides has been developed using a hypervalent iodine benziodoxole-derived cyano reagent. The procedure is accomplished within 10 min and without the use of any catalyst in DMF, at room temperature. Thus, the highly functionalized quaternary carbon-centered nitriles were produced in high to excellent yields.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/c4ob02032d | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!