Abstract
An efficient method has been developed for the asymmetric intramolecular C(sp3)−H amination of aryl and arylsulfonyl azides to give chiral indolines and benzofused cyclic sulfonamides in high product yields and with excellent enantioselectivities under mild reaction conditions, as reported by Li Dang, Yungen Liu, Chi-Ming Che and co-workers in their Research Article (e202218577). This method provides a complementary approach to asymmetric C(sp3)−H aminations by precious metal-based catalysis.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
