Abstract
Abstract Hydrido and hydroxyspirophosphoranes, cyclic tri-coordinated phosphorus compounds and a boron spirane involving a phenylenolpyruvate moiety were prepared from reactions between phenylpyruvic acid and phosphorus trichloride, or (and) chloro-2-dioxaphospholane 1,3,2, or (and) chloro-2-oxo-2-phenyl-4,5-dioxaphospholane 1,3,2, or (and) boric acid. The hydroxyphosphorane is a good model of the intermediate postulated in the hydrolysis of enolpyruvate phosphoric esters.
Sign-in/Register to access full text options 
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 callDisclaimer: 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.
