Abstract
Abstract Electrochemical propargylation of aldehydes and ketones with unsubstituted or α-substituted propargylic bromides using platinum cathode and zinc anode proceeded efficiently under mild conditions to give the corresponding homopropargyl alcohols exclusively in high yields. Similar electrochemical propargylation with γ-substituted propargyl bromides gave the corresponding homoallenyl alcohols as major products. Regioselectivity in the introduction of a propargyl or an allenyl group was controlled simply by a change of the anode material, zinc or aluminum.
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.
