Reactions of Early Transition Metal - Carbon Bonds with N-Heterocycles

被引:31
作者
Diaconescu, Paula L. [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
关键词
D O I
10.2174/138527208786241547
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Heterocycles are ubiquitous in biological compounds and methods to functionalize them have been of long standing interest. Reactions of early transition metal-carbon bonds with heterocycles are important in two major areas: ( 1) activation and functionalization of heterocycles and ( 2) ring-opening of aromatic heterocycles. In the first area, metal-carbon bonds determine ortho-metalation and insertion of unsaturated substrates to yield functionalized heterocycles. In the latter area, metal-element multiple bonds become important and provide the driving force for ring-opening reactions. This review will focus on reactions of nitrogen-containing heterocycles. Early transition metals are defined as elements belonging to groups III-V, the lanthanides, and the actinides; the reactivity of complexes featuring the metal in its highest oxidation state (d(0) f(n) electron count) and a carbon-based ligand will be described.
引用
收藏
页码:1388 / 1405
页数:18
相关论文
共 125 条
[1]   QUINOLINE BINDING MODE AS A FUNCTION OF OXIDATION-STATE IN ARYLOXIDE-SUPPORTED TANTALUM COMPLEXES - MODELS FOR HYDRODENITROGENATION CATALYSIS [J].
ALLEN, KD ;
BRUCK, MA ;
GRAY, SD ;
KINGSBOROUGH, RP ;
SMITH, DP ;
WELLER, KJ ;
WIGLEY, DE .
POLYHEDRON, 1995, 14 (22) :3315-3333
[2]   An overview of modeling studies in HDS, HDN and HDO catalysis [J].
Angelici, RJ .
POLYHEDRON, 1997, 16 (18) :3073-3088
[3]   Ring-enlargement and ring-opening reactions of benzoxazole, thiazoles, and benzisoxazole by zirconocene-alkyne complexes [J].
Arndt, P ;
Lefeber, C ;
Kempe, R ;
Rosenthal, U .
CHEMISCHE BERICHTE, 1996, 129 (02) :207-211
[4]   Alkyl complexes of rare-earth metals that contain a furyl-functionalized cyclopentadienyl ligand: Alkyl cation formation and unexpected ring-opening reaction of the furyl group [J].
Arndt, S ;
Spaniol, TP ;
Okuda, J .
ORGANOMETALLICS, 2003, 22 (04) :775-781
[5]   Mono(cyclopentadienyl) complexes of the rare-earth metals [J].
Arndt, S ;
Okuda, J .
CHEMICAL REVIEWS, 2002, 102 (06) :1953-1976
[6]   Formation of a dicationic yttrium η2-pyridyl complex from an yttrium methyl dication by C-H activation of pyridine [J].
Arndt, S ;
Elvidge, BR ;
Zeimentz, PM ;
Spaniol, TP ;
Okuda, J .
ORGANOMETALLICS, 2006, 25 (03) :793-795
[7]   Metalation of aromatic heterocycles by yttrium alkyl complexes that contain a linked amido-cyclopentadienyl ligand: synthesis, structure and Lewis base adduct formation [J].
Arndt, S ;
Trifonov, A ;
Spaniol, TP ;
Okuda, J ;
Kitamura, M ;
Takahashi, T .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2002, 647 (1-2) :158-166
[8]  
Arndt S, 2001, EUR J INORG CHEM, P73
[9]   SELECTIVE INTERMOLECULAR CARBON-HYDROGEN BOND ACTIVATION BY SYNTHETIC METAL-COMPLEXES IN HOMOGENEOUS SOLUTION [J].
ARNDTSEN, BA ;
BERGMAN, RG ;
MOBLEY, TA ;
PETERSON, TH .
ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (03) :154-162
[10]   Intermolecular C-H bond activation promoted by a titanium alkylidyne [J].
Bailey, BC ;
Fan, HJ ;
Baum, EW ;
Huffman, JC ;
Baik, MH ;
Mindiola, DJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (46) :16016-16017