posted on 2025-03-07, 12:48authored byYoussef Nassar, Fabien Rodier, Antony Bigot, Paul Cruciani, Vincent Ferey, Marc Daumas, Janine Cossy
A cross-coupling reaction between an enol triflate and
an aryl
Grignard reagent using a copper catalyst, followed by a deprotection
step, a Mitsunobu reaction, and a saponification, allowed for the
synthesis of Amcenestrant (SAR439859). This approach, avoiding an
expensive and toxic transition metal, is as efficient as the classical
route but less expensive for accessing this selective estrogen-receptor
degrader (SERD)