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  • Life and Medical Sciences  (13)
  • Palladium  (7)
  • 1995-1999  (14)
  • 1970-1974  (4)
  • 1950-1954
  • 1930-1934  (2)
  • 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.
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  • 2
    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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  • 3
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The developmental cycle of the teeth in Plethodon cinereus is analyzed on morphological grounds using alizarin preparations. All the stages in development do not occupy the same proportion of the life cycle time. Functional teeth and germs at an early stage in development occupy a large proportion of the life cycle time, whereas the processes of tooth shedding and ankylosis occur very quickly. The time during which any locus does not bear a functional tooth, and is therefore a non-functional locus, is reduced to a minimum. P. cinereus has a basic pattern of tooth replacement which is consistent with Zahnreihen which are 2.0 tooth spaces apart. Variations in the replacement pattern are common and these are produced by relatively small fluctuations in the spacing of the Zahnreihen around the „mean„ of 2.0. Localized disturbances which produce breaks in the replacement pattern and cause waves to cross also occur. These may be due to the failure of tooth germs to develop, the fusion of tooth germs, or may be the result of the inherent variability in a complex biological system. This variability causes individual tooth germs to develop too slowly or too quickly and hence assume an „abnormal“ position thus causing breaks in the replacement pattern. Tooth replacement may be controlled by an intra-local mechanism(s) rather than by stimuli which travel along the jaw.
    Additional Material: 8 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 136 (1972), S. 247-254 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The interspecific variation in the positional and mesenteric relationship of the mammalian oviduct to the ovary observed among 41 species is summarized by distinguishing eight morphological types of relationship. The recognition of types is based on wide species differences in: the position of the oviduct with reference to the mesosalpinxal fold and ovary; the extent to which oviducal mesenteries enclose the ovary in a periovarial sac; the degree of closure and method of formation of the peritoneal opening to the periovarial sac; and the morphology of the oviduct.
    Additional Material: 1 Ill.
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  • 5
    ISSN: 1434-1948
    Keywords: α-Metallated amino acids ; Palladium ; Platinum ; Oxidative addition ; α-Bromoglycinate ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidative addition of methyl N-benzoyl-2-bromoglycinate to bis(dibenzylideneacetone)palladium, in the presence of 2,2′-bipyridyl, and to (Ph3P)2Pt(η2-C2H4) gives the α-metallated glycine esters 1a and 2a. Abstraction of bromide from 1a, 2a, using AgSbF6 or AgBF4, affords the cationic C,O-chelate complexes [(bpy)Pd-CH(CO2Me)NHC(Ph)O]+ (1b,c) and [(Ph3P)2Pt-CH(CO2Me)NHC(Ph)O]+ (2b), respectively, featuring coordination of the amide O atom. The complexes 1b and 2b have been characterized by X-ray diffraction.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 93-99 
    ISSN: 1434-1948
    Keywords: 2-Methyl-1,2,3,4-tetrazole-5-thiolates ; 2-Phenyl-1,2,3,4-tetrazole-5-thiolates ; Palladium ; Platinum ; Copper ; Silver ; Gold ; Molecular structures ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The molecular structures of nine transition metal tetrazolethiolates have been determined by X-ray structure determinations. The ligand is invariably coordinated through its sulfur atom to the metal center [M = PdII, CuI, AgI, AuI, AuIII, and Hg]. The M-S-C bond angles vary considerably, but this cannot be correlated with variations in the C-S bond lengths. Intermolecular association occurs for Ph3PAu(SCN4Me) via Au-S contacts, leading to dimeric strands in the solid state. The copper compound (Ph3P)3Cu4(SCN4Me)4 (5), possesses a rather asymmetric structure: one Cu atom is tricoordinated by 3 sulfur atoms, the other three are tetracoordinated by P and N as well as by S atoms.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 471-482 
    ISSN: 1434-1948
    Keywords: Quinine ; Cinchonine ; Palladium ; Platinum ; Silver ; Gold ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of metal complexes in which quinine (L1) and cinchonine (L2) are coordinated via the four possible donor atoms was prepared and characterized. Coordination of the tertiary N atom of quinine is observed in [L1MPPh3]+NO3- [M = Au (1), Ag (2)], [L1Pd(COD)(Cl)]+ NO3- (3) and L1Pd(Cl)(allyl) (4). The mono anion of quinine functions as N,O chelate ligand in (L1-H+)M(Cl)(PR3) (M = Pd, Pt, 5-10), [(L1-H+)Pd(en)]+NO3- (11) and (L1-H+)2TiCl2 (12). Protection of the tertiary N atom of quinine by methylation or protonation allows the synthesis of the quinoline complexes [(L1CH3+)M(Cl)2(PR3)]+ BF4- (M = Pd, Pt, 14-18), [(L1CH3+)Ir(Cl)2(Cp*)]+ BF4- (19), [(L1+H+)M(Cl)2(PR3)]+ CF3SO3- (M = Pd, Pt, 20-22) and (L2+H+)(ZnCl3-) (23). Quinine and cinchonine act as N,O-N bridge in the complexes (R3P)(Cl)M(μ-L1-H+)M(Cl)2(PR3) (M = Pd, Pt, 24, 25, 27, 28), (Cp*)(Cl)Ir(μ-L1-H1)Ir(Cl)2(Cp*) (29), (EtP3)(Cl)Pd(μ-L2-H+)Pd(Cl)2(PEt3) (26), and as N-N bridge in the complexes [(Ph3P)Au(μ-L1)Au(PPh3)]+NO3- (30) and (allyl)(Cl)Pd(μ-L1)Pd(Cl)(allyl) (31). Coordination of quinine via the C=C double bond occurs in [(L1+2 H+)PtCl3]+Cl- (32). The structures of 11, 13, 19, 23, 26 and 32 were determined by X-ray diffraction. In most cases the coordination mode and the conformation of quinine can also be derived from the 1H-NMR spectra.
    Additional Material: 6 Ill.
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  • 8
    ISSN: 1434-1948
    Keywords: Palladium ; Azide ; Pyridine ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Palladium(II) azide (1) was synthesized by reaction of palladium nitrate and sodium azide. 1 was characterized by AAS, IR, and 14N-NMR spectroscopy. Bis(azido)bis(pyridine)palladium(II) (2) and tetramminepalladium tetraazidopalladate(II) (3) were synthesized by a high-yield reaction. Both were characterized by X-ray structural analysis, IR, Raman, and NMR spectroscopy.
    Additional Material: 4 Ill.
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  • 9
    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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  • 10
    ISSN: 0730-2312
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: We are using viral oncogene probes to study the pathways by which osteoblast-specific gene expression is induced in ascorbic acid-treated MC3T3-E1 cells. The 12S product of the adenovirus E1A gene binds directly to key cellular regulators and, as a result, represses tissue specific gene expression and blocks differentiation in a wide variety of cell types. The main cellular targets of the E1A 12S product are the pRB family and p300/CBP family. The p300 family appears to be the primary target for E1A-mediated repression of tissue-specific gene expression in a variety of cell types. We have generated MC3T3-E1 cell lines that stably express either the wild-type 12S product or a mutant that targets p300/CBP, but not the pRB family. Using these constructs to dissect osteoblast differentiation, we found that targeting of p300/CBP appears to be sufficient to repress alkaline phosphatase expression, although a low but functional level of expression can be maintained if the pRB family is not targeted as well. Induction of alkaline phosphatase expression and activity can be dissociated from expression of late-stage markers such as osteocalcin and osteopontin. Surprisingly, cell lines exhibiting severe repression of alkaline phosphatase activity differentiate to a mineral-secreting phenotype much like normal MC3T3-E1 cells. Osteopontin induction is dependent on at least a minimal level of alkaline phosphatase activity, although it is not dependent on induction of alkaline phosphatase at the RNA level. If alkaline phosphatase is supplied exogenously, osteopontin expression can be induced in conditions in which endogenous alkaline phosphatase is severely repressed. J. Cell. Biochem. 68:269-280, 1998. © 1998 Wiley-Liss, Inc.
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