Chemical and Pharmaceutical Bulletin p. 1885 - 1889 (1996)
Update date:2022-09-26
Topics:
Funayama, Shinji
Murata, Kiyoshi
Nozoe, Shigeo
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.
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