Abstract

Moreover, chiral selenideand diselenides containing ligands offer attractive and practical options in the development of asymmetric transformations. In this context, a straightforward synthesis of a new set of chiral β-seleno amine through a stereoselective aziridine ring opening with selenium nucleophiles, generated by reducing agents such as NaBH4, LiBHEt3, zinc or indium salts have been described by our group 2 . We herein report an ecofriendly procedure for the synthesis of chiral β-seleno amine under mild conditions, using selenium nucleophile generated by base in the presence of CuO nanopowder as a catalyst in ionic liquid BMIM[BF4] as solvent.

Full Text
Paper version not known

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 call

Disclaimer: 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.