## Abstract The synthesis of diorganotin(IV) derivatives of thiosalicylic acid, of 3‐aza‐2‐thiosalicylic acid, and of several related compounds is reported. Their characterization by ^__1__^H, ^__13__^C, and ^__119__^Sn NMR, Mössbauer, and mass spectrometry is described. The in vitro antitumor acti
Synthesis, characterization and in vitro antitumor activity of dimethyl-, diethyl, and di-t-butyl-tin(IV) derivatives of substituted salicylic acids
✍ Scribed by Mohammed Bouâlam; Rudolph Willem; Monique Biesemans; Marcel Gielen
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 551 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0268-2605
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✦ Synopsis
The synthesis of dimethyl-, diethyl-and/or di-tbutyl-tin(1V) derivatives of substituted salicylic acids of the type a, (X-Y-2-OH-C6H,C00) , 3-CH30; H, 5-CH30; 3-CH3, 6-(CH,),CH; 3,5-[(CH3)2CH]2 and 4,S-benzo) and b {[R2(X-Y-2-OH-C6H,COO)Sn]zO}2 (X, Y = H, 3,5-[(CH3),CH], and 4,S-benzo) is reported. Their characterization by 'H, I3C and 'I9Sn NMR, Mossbauer and mass spectrometry is described. The in uitro antitumor activity of selected derivatives against two human tumoral cell lines, MCF-7 and WiDr, is presented.
📜 SIMILAR VOLUMES
Values of coupling constants )2J("9Sn, 'H)), determined from 'H NMR spectra, gave estimates of C-Sn-C angles in Me,SnL in the range 128-136 O in methanol and aqueous solutions, which correspond to values from Il9Sn Mossbauer AE parameters (129.6-133.8 "). The structural relationship of R2SnL molecul