76474-95-8Relevant academic research and scientific papers
Solid-supported green synthesis of substituted hydrocinnamic esters by focused microwave irradiation
Kumar, Vinod,Sharma, Anuj,Sinha, Arun K.
, p. 483 - 495 (2006)
An efficient chemoselective hydrogenation protocol for substituted cinnamic esters is developed for the synthesis in quantitative yield of corresponding bioactive dihydrocinnamic esters with solid-supported palladium chloride/ammonium formate (cat.) in HCOOH/H2O 1:2 as a hydrogenating agent under focused-microwave irradiation for 10 min.
Synthesis of the core structure of acutumine
Reeder, Matthew D.,Srikanth,Jones, Spencer B.,Castle, Steven L.
, p. 1089 - 1092 (2007/10/03)
(Chemical Equation Presented) The tricyclic core of the bioactive natural product acutumine has been synthesized. Key steps include an oxidative phenolic coupling to form a masked o-benzoquinone, an anionic oxy-Cope rearrangement to construct an all-carbo
