Abstract

AbstractThe cover picture shows the mechanistic scheme of the synthesis of imidazo[1,5‐a]pyridinium salts from phenylchlorodiazirine and 2‐pyridyl Schiff bases. The carbene produced by thermolysis of the diazirine reacts with the pyridyl Schiff base to give two different ylide species, which are detected by laser flash photolysis. However, a single product is formed in a nearly quantitative yield and is easily separated from the reactants since it precipitates in nonpolar solvents. Colour code: blue = N, red = Cl, yellow = alkyl or aryl substituent, green = phenyl group. Details are discussed in the article by R. Bonneau and P. Guionneau on p. 5459 ff.

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.