Abstract
Stereochemical studies were performed on asymmetric [2, 3] sigmatropic rearrangements of sulfur ylides derived from chiral ketenimines possessing various kinds of substituents and prochiral sulfur ylides. A mechanistic pathway for these rearrangements is proposed on the basis of the stereochemical results obtained. New asymmetric centers are induced on the sulfur atoms of the ylides during the reactions.
Sign-in/Register to access full text options 
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.
