156953-83-2Relevant articles and documents
Absolute stereochemistry of (-)-preorixine and related compounds
Funayama, Shinji,Murata, Kiyoshi,Nozoe, Shigeo
, p. 1885 - 1889 (2007/10/03)
The absolute stereochemistry of the C-2' position of (-)-preorixine, postulated to be an important biosynthetic precursor of various quinoline alkaloids, was assigned as R by the combination of its chemical transformation and the extended Mosher method. The stereochemistry of the C- 2' position of (+)-orixine was also concluded to be R, establishing that no inversion occurred when (-)-preorixine was transformed into (+)-orixine.