Abstract
(E)-γ-Hydroxy and (E)-γ-keto-α,β-unsaturated sulfoxides have been easily prepared in good chemical yield from simple aldehydes 2 and chiral bis-sulfoxide 4 using a SPAC-type reaction. The onepot procedure is based on a Knoevenagel condensation, subsequent prototropic shift and [2,3] sigmatropic sulfoxide-sulfenate rearrangement.
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.
