Cycloaddition of Chiral tert-Butanesulfinimines with Trimethylenemethane
Organic Letters2013Vol. 15(8), pp. 2030–2033
Citations Over TimeTop 13% of 2013 papers
Abstract
The cycloaddition of chiral tert-butanesulfinimines with trimethylenemethane is found to give facile access to methylene-pyrrolidines with good yields and diastereoselectivities. The full scope of the cycloaddition is explored, and a range of transformations of the formed methylenepyrrolidines to give a range of functionalized chiral pyrrolidines is presented.
Related Papers
- → Palladium-Catalyzed [3 + 3] Cycloaddition of Trimethylenemethane with Azomethine Imines(2006)171 cited
- → Tandem Cycloaddition Reactions of Allenyl Diazo Compounds Forming Triquinanes via Trimethylenemethane Diyls(2011)39 cited
- → Cycloaddition of Chiral tert-Butanesulfinimines with Trimethylenemethane(2013)36 cited
- → Total Synthesis of Ceratopicanol through Tandem Cycloaddition Reaction of a Linear Substrate(2012)19 cited
- → Asymmetric [3+3] Cycloaddition of Trimethylenemethane with Nitrones(2007)