## Abstract magnified image In a search for cytotoxic fluorescent materials a series of Nβalkylated and N,Nβdialkylated 3,5βbis(arylidene)piperidones was synthesized. Alkylation of 3,5βbis(arylidene)β4βpiperidone afforded quaternary salts only while condensation of Nβalkylβ4βpiperidones with subst
N-phosphorylated 3,5-bis(arylidene)4-piperidones: Synthesis, X-ray structure, and evaluation of antitumor activity
β Scribed by Irina L. Odinets; Oleg I. Artyushin; Evgenii I. Goryunov; Konstantin A. Lyssenko; Ekaterina Yu. Rybalkina; Ilya V. Kosilkin; Tatiana V. Timofeeva; Mikhail Yu. Antipin
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 123 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.20147
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β¦ Synopsis
In a search for cytotoxic fluorescent ma- terials, a series of N-phosphorylated compounds 2a-c were prepared by phosphorylation of 3,5-bis(4-N,Ndimethylbenzylidene)-4-piperidone 1. According to X-ray investigations, molecule 2a is E,E-isomer with axial position of the P(O)(OCH 2 CF 3 ) 2 substituent. Fluorescence of compounds 2a-c was found to be similar to fluorescence of nonphosphorylated compound 1. The cytotoxicity of the compounds 2a-c was estimated on several human tumor cell lines (H9, K562, and MCF7).
π SIMILAR VOLUMES
A new series of N-phosphinylureas 5b, 6a-7c was synthesized and characterized by 1 H, 13 C, 31 P NMR, IR, and elemental analysis. The three-dimensional structure of 5b has been determined by X-ray crystallography. The crystal structure revealed the existence of four independent molecules. All struct
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v