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  • α-Amino acids  (4)
  • Iridium  (3)
  • 1
    ISSN: 0009-2940
    Keywords: Hexadeamino-hexaisocyano-neomycin B ; Organometallic complexes ; Gold ; Chromium ; Rhodium ; Iridium ; Ruthenium ; Palladium ; Platinum ; Hexanuclear carbene gold(I) complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From the amino glycoside neomycin B, the acetate-protected hexaisocyanide 4 has been prepared. 4 forms the hexanuclear complexes [(4)(AuCl)6] (5), {(4)[Cr(CO)5]6}, {(4)[MCl2(η5-C5Me5)]6} (M = Rh, Ir), {(4)[RuCl2(p-cymene)]6}, {(4)-[MCl2(PR3)]6} (M=Pd, Pt), and 4{(4)[PdCl(C6H4CH2NMe2)]6). The hexaisocyanohexagold(I) complex 5 reacts with H2NtBu and PhNH2 to give the corresponding carbene complexes. The compounds have been characterized by IR, 13C- and 31P-NMR spectroscopy, and (partially) by FAB-MS data.
    Additional Material: 4 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 1031-1034 
    ISSN: 0009-2940
    Keywords: Hexachloropalladate(IV) ; α-Amino acids ; 1-Pyrroline and 1-pyrroline-2-carboxylate as ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Complexes of Biologically Important Ligands, LI. - Reactions of α-Amino Acids with Hexachlorpalladate(IV). Stabilization of 1-Pyrroline at Palladium(II)Hexachloropalladate(IV) reacts with an excess of α-amino acids under reduction of the metal to give palladium(II) chelate complexes PdL2 (1) (L = anion of L-Val, L-Leu, L-Phe, L-Glu, L-Gln, DL-indoline-2-carboxylic acid). Chloro-bridged complexes LPd(μ-Cl)2PdL (2) are obtained from [PdCl6]2- and L-Asp, L-Asn, and L-thioproline, respectively. With L-Met, L-Cys, L-LeuOMe, and L-PheOMe Pd(II) complexes 3-5 are also isolated. L-Pro is dehydrogenated and decarboxylated by [PdCl6]2- to yield the Pd(II) complex 6 with 1-pyrroline-2-carboxylate and 1-pyrroline as ligands. L-Cys-Cys and L-Ala yield Pd(IV) complexes 8, 9.
    Notes: Hexachloropalladat(IV) setzt sich mit α-Aminosäuren im Überschuß unter Reduktion des Metalls zu Palladium(II)-Chelatkomplexen PdL2 (1) um (L = Anion von L-Val, L-Leu, L-Phe, L-Glu, L-Gln, DL-Indolin-2-carbonsäure). Chloro-verbrückte Palladium(II)-Komplexe LPd(μ-Cl)2PdL (2) bilden sich bei der Umsetzung von [PdCl6]2- mit L-Asp, L-Asn, und L-Thioprolin. Auch mit L-Met, L-Cys, L-LeuOMe und L-PheOMe werden Palladium(II)-Komplexe (3-5) isoliert. L-Pro wird durch [PdCl6]2- dehydriert bzw. decarboxyliert, wobei der Palladium(II)-Komplex 6 mit 1-Pyrrolin-2-carboxylat und dem in freiem Zustand instabilen 1-Pyrrolin als Liganden erhalten wird. L-Cys-Cys und L-Ala bilden Palladium(IV)-Komplexe (8, 9).
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  • 3
    ISSN: 0009-2940
    Keywords: Palladium complexes ; Rhodium complexes ; α-Amino acids ; 2-Iminocarboxylate as ligand ; Chiral glycine ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Biologically Important Ligands, LXVII[1]. - Synthesis of α-Amino Acids from Palladium(II)- and Rhodium(III)-Coordinated Imines and Oximes of α-OxocarboxylatesThe bis-chelate complexes Pd[O2CC(R1)=NOR2]2 (1) and Pd[O2CC(R1)=NR2]2 (2, R2 optically active substituent) are synthesized by template condensation of an α-oxocarboxylic acid with a hydroxylamine or amine component, respectively. Similarly, the Rh(III) complexes Cp*Rh(Cl)[O2CC(R)=N(CHMePh)] (3a: R = H, 3b: R = Me) were obtained from α-oxocarboxylic acids and optically active 1-phenylethylamine. Catalytic hydrogenation of 1 and 2 gives directly the free α-amino acids with, in case of 2, ee's between 0 and 36%. Nucleophilic attack by the carbanions of RC(O)CH2CO2Et and H2NCH(CO2Et)2 at the imino carbon atom of 3a leads to the α-amino carboxylato complexes 4 and 5. - Compounds 4a and 5 have been characterized by X-ray diffraction. Reaction of 3a with NaBH4 or NaBD4 followed by decomposition of the complex with HCl yields N-substituted glycine and N-substituted α-deuterio-glycine, respectively. The diastereoselectivity (70:30) of the α-deuteration could be determined by NMR spectroscopy.
    Additional Material: 2 Ill.
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  • 4
    ISSN: 0009-2940
    Keywords: Ruthenium complexes ; Osmium complex ; Hydrido complexes ; α-Amino acids ; Oxidative Addition ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Biologically Important Ligands, LXX[1].- Synthesis, Stereochemistry and Reactions of Ruthenium(II) and Osmium(II) Complexes with α-Amino CarboxylatesHerrn Professor Helmut Werner zum 60. Geburtstag gewidmet.The reactions of MHCl(CO)(PPh3)3 with salts of α-amino acids give the hydrido-N,O-chelate complexes MH(CO)(NH2CHR-COO)(PPh3)2 (1a-g;) M = Ru, Os). Complexes 1a-c can alternatively be prepared by oxidative addition of the appropriate α-amino acid to Ru(CO)3(PPh3)2. The crystal structure of 1b has been determined by an X-ray structural analysis. The leucinato compound 1c is an effective catalyst for the decomposition of formic acid. In contrast, reactions of RuHCl-(CO)(PPh3)3 with α-amino acids afford the chloro-N,O-che-late complexes RuCl(CO)(NH2CHRCOO)(PPh3)2 2a-h. The decomposition reactions of 2c, 2g and2h have been investigated.
    Additional Material: 2 Ill.
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  • 5
    ISSN: 0009-2940
    Keywords: Schiff bases ; Polyene dialdehydes ; α-Amino acids ; Pantamethylcyclopentadienyl complexes ; P ligands ; Iridium ; Palladium ; Platinum ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Schiff bases 1—11 were synthesized from α-amino acids or o-aminophenol and crocetindialdehyde, 2,7-dimethyloctatrienedial, terephthalaldehyde, or β,β′ -p-phenylendiacroleine. The reactions of these Schiff bases with chloro-bridged complexes [(R3P)(Cl)M(η-Cl)]2 (M = Pd, Pt) and [(C5Me5)(Cl)Ir(°Cl)]2 gave the dinuclear complexes 12-31.
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  • 6
    ISSN: 1434-1948
    Keywords: 2-Phenyl-4-R-5(4H)-oxazolones ; Iridium ; Palladium ; Platinum ; Iron ; Chromium ; C-o,N-Bridging 2-phenyloxazolone ; Peptide labelling ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of 2-phenyl-4-R-5(4H)-oxazolones (R = Me, CH2Ph, CHMeEt) with [(η5-C5Me5)IrCl2]2 afforded the cyclometallated complexes (η5-C5Me5)(Cl)Ir(L) (1-3) [L = 2-phenyl-4-R-5(4H)-oxazolone(C-o,N)]. 2-Phenyl-5(4H)-oxazolone reacts with [(η5-C5Me5)IrCl2]2 and palladium(II) acetate to give complexes with a C-o,N-bridging oxazolone [(η5-C5Me5)(Cl)Ir]2(μ-Cl)(μ-L-H+) (4) and Pd3(μ-ac)5(μ-L-H+) (5). 2-Phenyloxazolone anions were added to the π ligands of [(η5-C6H7)Fe(CO)3]+ and [(η7-C7H7)Cr(CO)3]+ to give the adducts 6-11. Dipeptide derivatives 12-18 were obtained by reaction of 1, 2 and by reaction of the adduct 6 from [(η5-C6H7)Fe(CO)3]+; and the anion of 2-phenyloxazolone with α-amino acid esters. These reactions may be used for the labelling of peptides. Saponification of 15-18 yields the organometallic substituted peptide acids 19-22. Their dianions (deprotonation of COOH and peptide amide) were used as ligands towards (Ph3P)2PtCl2 to yield the bimetallic complexes 23-25. The structures of 4, 5, 9 and 10 were determined by X-ray diffraction.
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