Herein, an efficient Lewis acid catalyzed protocol for the homo-Nazarov cyclizations of alkenyl cyclopropyl ketones is reported. Alkenes bearing β-hydrogens (or silyl groups) provide 1.5:1 mixtures of methylene cyclohexenols and cyclohexenones. When no β-hydrogens (or silyl groups) are present, only cyclohexenones are observed. Products are rapidly formed in good to high yields (up to 93%) under mild conditions and could be readily derivatized.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/ol102497w | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!