1400807-68-2Relevant academic research and scientific papers
Asymmetric total synthesis of smyrindiol employing an organocatalytic aldol key step
Enders, Dieter,Fronert, Jeanne,Bisschops, Tom,Boeck, Florian
, p. 1112 - 1117 (2012/09/08)
The first organocatalytic asymmetric synthesis of smyrindiol, by using an (S)-proline catalyzed enantioselective intramolecular aldol reaction as the key step, is described. Smyrindiol was synthesized from commercially available 2,4-dihydroxybenzaldehyde in 15 steps, with excellent stereoselectivity (de = 99%, ee = 99%). In the course of this total synthesis a new and mild coumarin assembly was developed.
