Abstract
Synthesis of novel C2-symmetric 1,2- 1,3- and 1,4- bis-sulfinamides and their use as effective ligands in rhodium (I) catalyzed asymmetric conjugate addition of arylboronic acids to cyclohexenone and cyclopentenones is described. C2-symmetry as well as chirality at the sulfur center in the ligand is crucial for the high enantioselectivity in the 1,4-addition reaction. It was also observed that the conjugate addition proceeded with good selectivity with Wilkinson's catalyst as the rhodium source.
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.
