Abstract
Abstract Regiospecific spiroalkylation of the selectively generated enolate arising from the 1,4-addition of lithium dimethylcuprate to 3-methylcyclohex-2-en-1-one allows an efficient preparation of spiroketones, including a key intermediate for the synthesis of (±)-α-Chamigrene.
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 callSimilar Papers
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.
