Abstract
Abstract The phosphorylation of tertiary alcohols can be performed only in some exceptional cases. We established, that phosphorylation of tertiary fluoroalkanols H(CF2) nCMe2OH (I, n = 2,4) with aryl- and polyfluoroalkyl-phosphorodicnlor-idates or aryl- and alkylphosphonic dichlorides in the presence of metal of metal salt catalysts yields chloroan-hydrides (II) and (III). When benzyl phosphorochloridates (IV) are used as phosphorylating agents, either products of phosphorylation or products of alkylation are formed depending on the nature of the substituent in the aromatic ring.
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 callMore From: Phosphorus, Sulfur, and Silicon and the Related Elements
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.
