32317-16-1Relevant academic research and scientific papers
Radical conjugate addition of aryl-tethered -alkoxyacrylates: Formal synthesis of (±)-Frenolicin B and (±)- epi -Frenolicin B
Donner, Christopher D.
experimental part, p. 415 - 420 (2010/04/26)
The radical conjugate addition of aromatic-tethered O-stannyl ketyl radicals to -alkoxyacrylates is demonstrated for the preparation of benzopyran - lactone-fused tricyclic systems. This method is then applied to the stereodivergent formal synthesis of th
Molecular clips based on propanediurea. Exceptionally high binding affinities for resorcinol guests
Jansen,De Gelder,Rowan,Scheeren,Nolte
, p. 2643 - 2653 (2007/10/03)
A series of new receptor molecules derived from 2,4,6,8-tetraazabicyclo[3.3.1]nonane-3,7-dione (propanediurea) is described. These molecules possess a cavity which is defined by two nearly parallel aromatic side walls positioned on top of a bis-urea frame
Synthesis, X-ray structure and binding properties of molecular clips based on dimethylpropanediurea
Jansen, Rob J.,Rowan, Alan E.,De Gelder, Rene,Scheeren, Hans W.,Nolte, Roeland J. M.
, p. 121 - 122 (2007/10/03)
New concave host molecules show strong noncovalent binding of hydroxybenzene derivatives by an induced fit mechanism (Ka up to 3.4 × 106 dm3 mol-1).
