Abstract
The facile synthesis of furopyridine (VIII) is achieved in five steps from the known piperidinone (I) via Wittig olefination, intramolecular cyclization of (III) by treatment with Ph-Se-Cl, NaJO4-mediated oxidative dehydroselenylation, furan ring formation by reduction, and finally, aromatization.
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.
