Convenient synthesis, characterization and GPx-like catalytic activity of novel ebselen derivatives

被引:61
作者
Zade, SS [1 ]
Panda, S
Tripathi, SK
Singh, HB
Wolmershäuser, G
机构
[1] Indian Inst Technol, Dept Chem, Bombay 400076, Maharashtra, India
[2] Univ Kaiserslautern, Fachbereich Chem, D-67653 Kaiserslautern, Germany
关键词
ebselen; nonbonding interactions; benzisochalcogenazolone; Te-N heterocycles; ortho-lithiation;
D O I
10.1002/ejoc.200400326
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis and characterization of benzisochalcogenazolones (ebselen derivatives 16-21) is described. The synthesis of 16-21 was achieved by treating the bromo precursors 11-13 with an appropriate dilithium dichalcogenide. The synthesis of benzisoselenazolones 16 and 18 was also accomplished by an alternative route, that is, by treating the corresponding methoxymethyl selenides 22 and 23 with 1 equiv. of bromine. The synthesis of methoxymethyl selenides 22 and 23 was accomplished by lithiation of the bromo precursors followed by treatment with bis(methoxymethyl) diselenide. The benzisoselenazolones 16 and 17 were characterized by single-crystal X-ray techniques. The GPx-like catalytic activities of compounds 16-18 and 21 were determined by using the coupled reductase assay. Compound 16 was found to be less active than ebselen 8 whereas compounds 17 and 18 were more active than ebselen in this assay. Compound 21 showed a 1.5-fold higher activity than its selenium analogue 17. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004).
引用
收藏
页码:3857 / 3864
页数:8
相关论文
共 73 条
[1]   Asymmetric methoxyselenenylations and cyclizations with 3-camphorseleno electrophiles containing oxime substituents at C-2. Formation of an unusual oxaselenazole from an oxime-substituted selenenyl bromide [J].
Back, TG ;
Moussa, Z ;
Parvez, M .
JOURNAL OF ORGANIC CHEMISTRY, 2002, 67 (02) :499-509
[2]   A novel camphor-derived selenenamide that acts as a glutathione peroxidase mimetic [J].
Back, TG ;
Dyck, BP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (09) :2079-2083
[3]   Solution and solid state studies of some new silicon and germanium compounds stabilized by tridentate ligands [J].
Benin, VA ;
Martin, JC ;
Willcott, MR .
TETRAHEDRON, 1997, 53 (29) :10133-10154
[4]  
Bien Malgorzata, 1999, Archivum Immunologiae et Therapiae Experimentalis, V47, P185
[5]   A novel ferrocenyl diselenide for the catalytic asymmetric aryl transfer to aldehydes [J].
Bolm, C ;
Kesselgruber, M ;
Grenz, A ;
Hermanns, N ;
Hildebrand, JP .
NEW JOURNAL OF CHEMISTRY, 2001, 25 (01) :13-15
[6]   SYNTHESIS AND CHARACTERIZATION OF STERICALLY ENCUMBERED LI, NA, AND K-ARYL TELLUROLATES, AND SOME PT(II), IR(I), AND CD(II) DERIVATIVES [J].
BONASIA, PJ ;
ARNOLD, J .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1993, 449 (1-2) :147-157
[7]  
CHANDIERE J, 1998, PHOSPHORUS SULFUR, V136, P467
[8]   Pyridineselenolate complexes of copper and indium: Precursors to CuSex and In2Se3 [J].
Cheng, Y ;
Emge, TJ ;
Brennan, JG .
INORGANIC CHEMISTRY, 1996, 35 (25) :7339-7344
[9]   Pyridineselenolate complexes of tin and lead: Sn(2-SeNC5H4)(2), Sn(2-SeNC5H4)(4), Pb(2-SeNC5H4)(2), and Pb(3-Me(3)Si-2-SeNC5H3)(2). Volatile CVD precursors to group IV group VI semiconductors [J].
Cheng, YF ;
Emge, TJ ;
Brennan, JG .
INORGANIC CHEMISTRY, 1996, 35 (02) :342-346
[10]   POLYMERIC CD(SE-2-NC5H4)2 AND SQUARE-PLANAR HG(SE-2-NC5H4)2 - VOLATILE CVD PRECURSORS TO II-VI SEMICONDUCTORS [J].
CHENG, YF ;
EMGE, TJ ;
BRENNAN, JG .
INORGANIC CHEMISTRY, 1994, 33 (17) :3711-3714