Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 9, Issue 1, Pages 74-77Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c0ob00699h
Keywords
-
Categories
Funding
- National Natural Science Foundation of China [20872166]
Ask authors/readers for more resources
Ahighly diastereoselective three-component inverse-electron-demand aza Diels-Alder reaction assisted by per(poly) fluoroalkanesulfinamides is presented, providing a broad spectrum of highly functionalized piperidine derivatives with excellent endo/exo and facial diastereoselectivities. The electron-withdrawing perfluoroalkyl groups are crucial for the success of this reaction under mild conditions and facilitate monitoring the process and stereoselectivities of the reaction. The synthetic potential of these cycloadducts is also highlighted.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available