Abstract

(Perhaloaryl)dimethylsilanes undergo a cleavage reaction with organolithium compounds, using very moderate conditions, to produce (perhaloaryl)lithium derivatives in good yield. ▪ The corresponding trimethylsilyl compounds [except for 2,5-bis(trimethylsilyl)dichlorothiophene] and phenyldimethylsilane were not cleaved significantly.

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.