70550-46-8Relevant articles and documents
Synthesis of diastereoisomeric 1,2,3-triphenylindans
Alesso, Elba N.,Finkielsztein, Liliana M.,Lantano, Beatriz,Bianchi, Daniel E.,Moltrasio Iglesias, Graciela Y.,Aguirre, Jose M.
, p. 149 - 152 (2007/10/03)
The stereoisomers of 1,2,3-triphenylindans were synthesized via 1,2,3-triphenylindan-1-ols. The configurational assignments of all the compounds were made by chemical and spectroscopic methods. An unexpected compound was isolated as a by-product of the Gr
Electrochemical Reduction of Activated Carbon-Carbon Double Bonds. Part 2. Mechanism and Stereochemistry of the Reduction of Self-protonating Indenes
Farnia, Giuseppe,Sandona, Giancarlo,Marcuzzi, Franco,Melloni, Giovanni
, p. 247 - 254 (2007/10/02)
The reduction at a mercury electrode in dimethylformamide of five variously substituted indenes bearing at least one (acidic) hydrogen at C(1) was carried out, under self-protonation conditions and in the presence of phenol as a proton donor.Reduction occ
