STUDIES ON THE ORAL ANTICANCER DRUG JM-216 - SYNTHESIS AND CHARACTERIZATION OF ISOMERS AND RELATED COMPLEXES

Citation
Cfj. Barnard et al., STUDIES ON THE ORAL ANTICANCER DRUG JM-216 - SYNTHESIS AND CHARACTERIZATION OF ISOMERS AND RELATED COMPLEXES, Inorganic chemistry, 35(11), 1996, pp. 3280-3284
Citations number
25
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201669
Volume
35
Issue
11
Year of publication
1996
Pages
3280 - 3284
Database
ISI
SICI code
0020-1669(1996)35:11<3280:SOTOAD>2.0.ZU;2-0
Abstract
The complex cis, trans, cis-[PtCl2(OAc)(2)NH3(c-C6H11NH2)] (JM-216) is currently undergoing clinical evaluation as an antitumor agent. In su pport of characterization and analysis of this complex a study of its isomers and other complexes [PtClm(OAc)((4-m))NH3(c-C6H11NH2)] (m = 0- 4) has been undertaken. The complexes have been obtained by a variety of synthetic routes which now extend the scope for the preparation of platinum(IV) antitumor complexes. As platinum(IV) complexes are very s table to substitution in the absence of catalysis, use has been made o f both light and base catalysis to promote substitution. Oxidative add ition to platinum(II) using hypervalent iodine reagents has also been used. The stereochemistry of the complexes has been confirmed by spect roscopic studies, primarily NMR including natural abundance N-15 NMR s pectroscopy.