475598-39-1Relevant academic research and scientific papers
Metal-free, regio- and stereoselective synthesis of linear (E)-allylic compounds using C, N, O, and S nucleophiles
Huang, Xiaojun,Fulton, Brandon,White, Kana,Bugarin, Alejandro
supporting information, p. 2594 - 2597 (2015/06/16)
A variety of allylic acetates and derivatives were synthesized by an efficient two-step protocol that employs readily available terminal alkenes as starting materials. This method is highly regio- and stereoselective, affording the linear (E)- isomer as the sole adduct. This process tolerates several functional groups including halogen-containing molecules, and it is general for weak oxygen, carbon, nitrogen, and sulfur nucleophiles. Furthermore, adducts were obtained in good to excellent yields.
The constituents and synthesis of cryptamygin-A from the stem bark of Cryptocarya amygadalina
Chan, Yu-Yi,Wu, Chia-Hung,Wu, Shwu-Jen,Wu, Tian-Shung
, p. 263 - 268 (2007/10/03)
Three new benzenoid compounds, namely cryptamygin-A, -B and -C together with eleven known compounds were isolated from the stem bark of Cryptocarya amygadalina. Their structures were elucidated by spectral analysis. The synthesis of cryptamygin-A is also
