1346113-24-3Relevant academic research and scientific papers
An inverse electron-demand diels-alder-based total synthesis of urolithin M7
Pottie, Ian R.,Nandaluru, Penchal Reddy,Bodwell, Graham J.
, p. 2245 - 2247 (2011)
Urolithin M7 was synthesized from 2-hydroxy-4-methoxybenzaldehyde in 8 steps and 48% overall yield. The key step was an inverse electron demand Diels-Alder (IEDDA) reaction between diene 10 and the enamine (7) derived from dimethoxyacetaldehyde and pyrrolidine, which generated the 6H-dibenzo[b,d]pyran- 6-one skeleton. Georg Thieme Verlag Stuttgart - New York.
