935549-58-9Relevant academic research and scientific papers
Highly stereoselective [4 + 3] cycloadditions of nitrogen-stabilized oxyallyl cations with pyrroles. An approach to parvineostemonine
Antoline, Jennifer E.,Hsung, Richard P.,Huang, Jian,Song, Zhenlei,Li, Gang
, p. 1275 - 1278 (2008/01/01)
Figure presented A highly stereoselective [4 + 3] cycloaddition of N-substituted pyrroles with allenamide-derived nitrogen-stabilized chiral oxyallyl cations is described here. This method provides an approach for constructing tropinone alkaloids.
