A new strategy for cyclopenta[]furan synthesis mediated by hypervalent iodine(III) has been described. The approach employs diacetoxyiodobenzene-induced initial dehydrogenation to a putative trienone intermediate and triggered sequential cycloisomerization to form the cyclo-penta[]furan targets.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274509 | PMC |
| http://dx.doi.org/10.3390/molecules21121713 | DOI Listing |
Publication Analysis
Top Keywords
hypervalent iodineiii-induced
4
iodineiii-induced domino
4
domino oxidative
4
oxidative cyclization
4
cyclization synthesis
4
synthesis cyclopenta[b]furans
4
cyclopenta[b]furans strategy
4
strategy cyclopenta[]furan
4
cyclopenta[]furan synthesis
4
synthesis mediated
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!