Abstract
AbstractAn efficient and convenient methodology for the formation of 2,3‐dihydro[1,3]thiazolo[3,2‐a]pyridinium derivatives is developed, which is based on the interaction of alkenes with sulfenylating reagents generated by the action of sulfuryl chloride or antimony pentachloride on di(2‐pyridyl)disulfide (I).
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.
