Abstract
AbstractIbogamine (11b) was synthesized starting from the vinyl sulfone 3. Addition of organocuprate reagents to 3 furnished 2a–d with high stereoselectivity. Only products from the syn addition of the cuprate reagents could be detected. Functional group transformations provided 7a,b the key intermediates for the synthesis of (±)‐21‐noribogamine (11a) and (±)‐ibogamine (11b).
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
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
