Abstract
Synthesis of 1,8‐naphthyridine‐annulated polyheterocycles containing oxygen, nitrogen, and sulfur has been achieved by thionation and sequential Claisen rearrangement of 4‐(4′‐aryloxybut‐2′‐ynyloxy)‐1‐phenyl[1,8]‐naphthyridin‐2‐ones first by heating in 1,2‐dichlorobenzene for 1–2 h and then by anhydrous AlCl3‐catalyzed Claisen rearrangement in dichloromethane for 1 h.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: 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.