A metal-free intramolecular borylative cyclization of 1,6-allenynes driven by BCl was developed. This method provides a general and practical strategy to construct valuable pyrrolidines containing all-carbon quaternary centers or 3,5-dihydroazepine derivatives depending on the substituents of the allene, with conjugative and sterically hindered phenyl groups favoring the latter.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.1c03062 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!