97006-05-8Relevant academic research and scientific papers
Diastereoselective synthesis of substituted hexahydrobenzo[de]isochromanes and evaluation of their antileishmanial activity
Saikia, Anil K.,Sultana, Sabera,Devi, Ngangbam Renubala,Deka, Manash J.,Tiwari, Kartikeya,Dubey, Vikash K.
supporting information, p. 970 - 979 (2016/01/15)
Hexahydrobenzo[de]isochromanes and hexahydropyrano[3,4,5-ij]isoquinolines can be efficiently synthesized via Friedel Crafts and oxa Pictet-Spengler reaction of acrylyl enol ethers mediated by triflic acid in good yields. The reaction is highly stereoselective. Two of the hexahydrobenzo[de]isochromanes are found to have moderate antileishmanial activity.
Sila-rhubafuran and derivatives: Synthesis and olfactory characterization of novel silicon-containing odorants
Foerster, Bettina,Bertermann, Ruediger,Kraft, Philip,Tacke, Reinhold
, p. 338 - 346 (2014/02/14)
Sila-rhubafuran (1b), a silicon analogue of the grapefruit odorant rhubafuran (1a), was synthesized and isolated as a 1:1 mixture of two racemic diastereomers. In addition, the structurally related racemic C/Si pairs 2a/2b and 3a/3b were prepared. To get
