332095-63-3Relevant academic research and scientific papers
Elucidation of the stereostructure of the annonaceous acetogenin (+)-montecristin through total synthesis
Harcken,Brueckner
, p. 40 - 54 (2007/10/03)
Total syntheses of ent-5-epi-montecristin (1a) and of (-)-montecristin (1b) were accomplished. The stereocenters of compounds 1a and 1b were established by asymmetric dihydroxylations of the trans-configurated β,γ-unsaturated esters 6 (→4, up to 80% ee; S
