A di-tert-butyl peroxide (DTBP)-promoted difunctionalization of α-aryl α-alkynyl allylic alcohols with alkyl nitriles was developed, affording a series of α-alkynyl γ-cyano functionalized ketones in moderate yields. This procedure involved C(sp)-H bond cleavage of alkyl nitriles and radical 3-exo-dig cyclization. After this, radical 1,2-alkynyl migration is preferred rather than 1,2-aryl migration.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/d1ob00192b | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!