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  • Inorganic Chemistry  (2)
  • [abr] CSNB; congential stationary night blindness  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Molecular genetics of inherited retinal degenerations
    Amsterdam : Elsevier
    Current Opinion in Genetics & Development 2 (1992), S. 459-466 
    Details
    ISSN: 0959-437X
    Keywords: [abr] AIED; Aland island eye disease ; [abr] CSNB; congential stationary night blindness ; [abr] HR; hereditary retinoschisis ; [abr] OA; ocular albinism ; [abr] OAT; ornithine aminotransferase ; [abr] OED; Oregon eye disease ; [abr] RP; retinitis pigmentosa ; [abr] RS; retinoschisis ; [abr] TCD; tapetochoroidal dystrophy ; [abr] XL; X-linked ; [abr] YAC; yeast artificial chromosome ; [abr] ad; autosomal dominant ; [abr] ar; autosomal recessive
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1016/S0959-437X(05)80158-3
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Molecular genetics of inherited retinal degenerations
    Amsterdam : Elsevier
    Current Opinion in Genetics & Development 2 (1992), S. 459-466 
    Details
    ISSN: 0959-437X
    Keywords: [abr] AIED; Aland island eye disease ; [abr] CSNB; congential stationary night blindness ; [abr] HR; hereditary retinoschisis ; [abr] OA; ocular albinism ; [abr] OAT; ornithine aminotransferase ; [abr] OED; Oregon eye disease ; [abr] RP; retinitis pigmentosa ; [abr] RS; retinoschisis ; [abr] TCD; tapetochoroidal dystrophy ; [abr] XL; X-linked ; [abr] YAC; yeast artificial chromosome ; [abr] ad; autosomal dominant ; [abr] ar; autosomal recessive
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1016/S0959-437X(05)80158-3
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Structural Studies on Indium and Tin Thiobenzoates (1996)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 1093-1098 
    Details
    ISSN: 0009-2940
    Keywords: Indium tris(thiobenzoate) ; Triethylammonium tetrakis(thiobenzoato)indate ; Tin, butyl-, tris(thiobenzoate) ; Tin, dichloro-, bis(thiobenzoate) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Indium(III) and tin(IV) thiocarboxylates were prepared and characterized on the basis of their IR, 13C- and 19Sn-NMR data. Indium tris(thiobenzoate) (1) decomposes into a sulfido complex In (S)[S(O)CPh] (2a). The corresponding tris(thioacetate) In[S(O)CMe]3 is thermally too unstable to be isolated. The anionic tetrakis complex [Et3NH]{In[S(O)CPh]4} (3) was characterized by X-ray crystallography which revealed a distorted tetrahedral coordination at the In atom. X-ray diffraction analysis of the complexes BuSn[S(O)CPh]3 (4) and Cl2Sn[S(O)CPh]2 (7) showed distorted tetrahedral and cis-octahedral structures, respectively.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19961290918
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Tetra o-Tolyltin and its Halogen Derivatives (1966)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 344 (1966), S. 102-106 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Tetra-o-tolylzinn wurde in 45proz. Ausbeute mit Hilfe der Wurtz-Reaktion (Petroläther als Lösungsmittel; Hg als Katalysator) dargestellt. Durch Jodierung wurden daraus Tri-o-tolylzinnjodid und Di-o-tolylzinndijodid erhalten; ferner gelang die Darstellung von Tri-o-tolylzinnfluorid.
    Notes: Tetra-o-tolyltin has been prepared in 45% yield for the first time by Wurtz reaction. Optimum yield is obtained using pet-ether (b. p. 65-85) as solvent and small amounts of mercury as catalyst. A mechanism for the role of mercury in the reaction is suggested. Tri-o-tolyltin iodide and hitherto unknown di o-tolyltin di-iodide have been prepared in 65% and 55% yields respectively by controlled iodination of the compound. Tri o-tolyltin fluoride has also been synthesised for the first time in almost quantitative yield.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19663440114
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    Paper (German National Licenses)
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