A Highly Stereoselective Total Synthesis of the Natural Enantiomer of Olivin

DOI: 10.1021/ja00258a077

Source and publish data:

Journal of the American Chemical Society p. 7575 - 7577 (1987)

Update date:2022-08-04

Topics: Regioselectivity   Column chromatography   Yield   NMR spectroscopy   Catalyst   Enantiomeric excess (ee)   Recrystallization   Total synthesis   Rotary evaporation   Stereoselective   TLC (thin-layer chromatography)   HPLC (high-performance liquid chromatography)   Protecting group   Anhydrous conditions   Retrosynthetic analysis   Workup   Chiral Auxiliary   Inert atmosphere   Natural enantiomer  

Authors:

Roush, William R.

Michaelides, Michael R.

Tai, Dar Fu

Chong, Wesley K. M.