186693-85-6Relevant articles and documents
Electron transfer-initiated Diels-Alder cycloadditions of 2′-hydroxychalcones
Cong, Huan,Ledbetter, Dustin,Rowe, Gerard T.,Caradonna, John P.,Porco Jr., John A.
, p. 9214 - 9215 (2008)
An efficient approach to cyclohexenyl chalcones employing highly electron rich 2′-hydroxychalcone dienophiles via electron transfer-initiated Diels-Alder cycloaddition is described. Using the methodology, the total synthesis of nicolaiodesin C has been accomplished. Copyright
Syntheses of knerachlin A and knerachlin B
Huang, Chusheng,Da, Shijun,Li, Ying,Li, Yulin
, p. 277 - 278 (2007/10/03)
The first total syntheses of knerachlin A and knerachlin B are described, starting from 2,4,6-trihydroxyacetophenone and 2,6- dihydroxyacetophenone, respectively. The key step in the synthesis is the condensation of ketone 5 with cinnamaldehyde.