Abstract
Abstract Arynes, generated in situ from o-(trimethylsilyl)aryl triflates by treatment with a fluoride, have been shown to react efficiently with various alkoxyphosphines via a mechanism similar to the Michaelis–Arbuzov reaction. Diverse aromatic oxophosphorus compounds, including derivatives with an ortho-ester function, have become easily available from a common aryne precursor by this method.
Full Text
Published Version (
Free)
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