C. Kunick et al., 2-substituted paullones: CDK1/cyclin B-inhibiting property and in vitro antiproliferative activity, BIOORG MED, 10(6), 2000, pp. 567-569
9-Trifluoromethyl-paullones with a carbon chain in the 2-position were synt
hesized by palladium-catalyzed coupling reactions of a 2-iodoprecursor with
terminal alkenes or alkynes, respectively. The introduction of a 2-cyanoet
hyl substituent led to a significant enhancement of CDK1/cyclin B inhibitin
g property and in vitro antiproliferative activity. (C) 2000 Elsevier Scien
ce Ltd. All rights reserved.