Abstract

Cycloaddition of acylketenes (2) to 1, 2-and 1, 3-dipolar compounds was investigated. The thermal reaction of 1, 3-dioxin-4-ones (1) with isoquinolinium phenacylide (11) gave the aromatized pyrrolo [2, 1-a] isoquinolines (12-15). The reaction of 1 with pyridinium and isoquinolinium cyanomethylides (3-5) afforded the 1, 3-oxazinylmethylides (6-8). The intermediate 2 likewise reacted with cyanamides and benzonitriles to give the corresponding 1, 3-oxazin-4-one derivatives (19-23).

Full Text
Paper version not known

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 call

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.