The aza-analogue of cephalotaxine skeleton has been prepared by series of reactions which include a 1,3-dipolar cycloaddition in 100% diastereoselectivity.
ASJC Scopus subject areas
- Drug Discovery
- Organic Chemistry
Nyerges, M., Bitter, I., Kádas, I., Tóth, G., & Toke, L. (1994). 1,3-dipolar cycloaddition approach towards the stereoselective preparation of aza-cephalotaxine skeleton. Tetrahedron Letters, 35(25), 4413-4414. https://doi.org/10.1016/S0040-4039(00)73370-3