Abstract

A simple, novel synthesis of (E)-gem-dimetalloalkenes containing boron and silicon based on (Z)-1-bromo-1-alkenyl-boronate esters is developed. 1-Bromo-(Z)-1-alkenylboronate esters readily available from literature procedures smoothly undergo a reaction with trimethylsilyllithium (easily generated from hexamethyldisilane with methyllithium in hexamethylphosphoramide) to provide the corresponding 'ate' complexes. These 'ate' complexes undergo intramolecular nucleophilic substitution reaction to provide the corresponding (E)-1-alkenylboronate esters containing trimethylsilyl moiety in good isolated yields (72-85%). The carbon skeletons present in these intermediates are confirmed by oxidation to the corresponding alkyl trimethylsilyl ketones with sodium acetate and hydrogen peroxide.

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.