Journal
ORGANIC LETTERS
Volume 12, Issue 9, Pages 2140-2141Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol100652b
Keywords
-
Categories
Ask authors/readers for more resources
The phenanthroindolizidine alkaloid (S)-(+)-tylophorine was synthesized from L-proline in nine linear steps including a double bromination and a free-radical cyclization of an N-aziridinylimine as the key steps. The phenanthrene moiety was prepared from homoveratric acid and veratraldehyde and permits the variation of each oxygen-substituted ring.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available