High value oxygenated polycycles have been rapidly and efficiently accessed from simple precursors in one pot processes. The reported methodology relies on a new and mild method for butenolide synthesis mediated by thiols. The initial photooxygenation and butenolide synthesis have been merged with subsequent photoredox reactions to achieve rare dual-photocatalyst cascades affording various fused butyrolactones. Ground state Lewis acid activity for methylene blue has been unveiled and then exploited in the synthesis of substituted cyclopentanones.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.2c03513 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!