22161-36-0Relevant articles and documents
Synthesis and biological evaluation of some stilbene derivatives
Karki, Subhas Somalingappa,Bhutle, Santosh Ramarao,Sahoo, Subhas,Reddy, Ratnakar,Balzarini, Jan,De Clercq, Erik,Darji, Satyanarayana Y.
experimental part, p. 1349 - 1356 (2012/05/05)
Several trans and cis stilbenes with substitution n the olefinic bridge were synthesized and characterized by IR, NMR and mass spectroscopy in an effort to obtain ubstances that could be more readily formulated. All the synthesized compounds were screened against Molt4/C8, CEM and L1210 cell lines. None of these compounds were ndowed with pronounced cytostatic activity. However,Schiff derivatives emerged as cytostatic agents (IC50: 0.77-10 μg/ml) that deserve further investigation. Springer Science+Business Media, LLC 2010.
Reactions of Halogenated α-Phenylcinnamic Acids with Potassium Amide in Liquid Ammonia : Part I - Reactions of cis- and trans-2-Chloro-α-phenylcinnamic Acids
Kessar, S. V.,Nadir, U. K.,Gupta, Y. P.,Pahwa, P. S.,Singh, Paramjit
, p. 1 - 3 (2007/10/02)
Reaction of trans- and cis-2-chloro-α-phenylcinnamic acids (1) with KNH2 in liquid ammonia gives phenanthrene-9-carboxylic acids (2) and 3-phenylcarbostyrils (8).Under similar conditions 3-chloro-α-phenylcinnamic acids (5) furnish 3-phenylcoumarins (6).
