Zobrazeno 1 - 10
of 62
pro vyhledávání: '"W, Aicher"'
Autor:
W. Aicher, F.B. Maurer, L. Reitnauer, M. Korn, M. Maas, J. Hennenlotter, T. Todenhöfer, A. Stenzl
Publikováno v:
European Urology Open Science, Vol 19, Iss , Pp e416- (2020)
Externí odkaz:
https://doaj.org/article/44e819d92ed947b1a42dd7db908f5d1f
Autor:
Max Widemann, Frederik S. W. Aicher, Martin Bonath, Klaus Eichele, Cäcilia Maichle‐Mössmer, Hartmut Schubert, Peter Sirsch, Reiner Anwander, Lars Wesemann
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 28(45)
Following the alkane-elimination route, the reaction between tetravalent aryl tintrihydride Ar*SnH
Autor:
N, Harland, B, Amend, N, Lipke, S Y, Brucker, F, Fend, A, Herkommer, H, Lensch, O, Sawodny, T E, Schäffer, K, Schenke-Layland, C, Tarín Sauer, W, Aicher, A, Stenzl
Publikováno v:
Der Urologe. Ausg. ALiteratur. 60(9)
In the context of cancer surgery, there is always a trade-off between oncological safety and preservation of function. This is especially true in pelvic surgery due to the close relationship to the pelvic floor muscles, blood supply and nerves. Curre
Publikováno v:
Organometallics. 37:1773-1780
Adamantylisonitrile and benzonitrile were reacted with bulky substituted organotin trihydride [Ar*SnH3] [Ar* = (C6H3-2,6-Trip2), Trip = 2,4,6-triisopropylphenyl]. They do not show any reaction at room temperature as well as at 80 °C. After activatio
Publikováno v:
Angewandte Chemie. 129:2232-2236
Ein sterisch anspruchsvoll substituiertes Stannan Ar*SnH3 (Ar*=2,6-(2′,4′,6′-Triisopropylphenyl)phenyl) wurde mit dem bekannten frustrierten Lewis-Paar (FLP) PtBu3/B(C6F5)3 in verschiedenen stochiometrischen Zusammensetzungen umgesetzt. Unter a
Autor:
Frederik S. W. Aicher, Christian P. Sindlinger, Jakob-Jonathan Maudrich, Hartmut Schubert, Klaus Eichele, Lars Wesemann
Publikováno v:
Chemistry - A European Journal. 23:2192-2200
Alkyltin trihydride [(Me3 Si)2 CHSnH3 ] was synthesized and the reductive elimination of hydrogen from this species was investigated. A methyl-substituted N-heterocyclic carbene reacts with the organotrihydride in dependence on stoichiometry and solv
Autor:
Lars Wesemann, Frederik S. W. Aicher, Klaus Eichele, Fatima Diab, Christian P. Sindlinger, Hartmut Schubert
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(17)
Bulkily substituted organodihydrogermylium and -stannylium cations [Ar*EH2 ]+ (E=Ge, Sn; Ar*=2,6-Trip2 C6 H3 , Trip=2,4,6-triisopropylphenyl) were characterized as salts of the weakly coordinating perfluorinated alkoxyaluminate anion [Al{OC(CF3 )3 }4
Publikováno v:
Inorganic chemistry. 56(1)
The reaction of MeNHC (MeNHC = 1,3,4,5-tetramethylimidazolylidene, where NHC = N-heterocyclic carbene) adducts to organotin(II) hydrides Ar*SnH and Ar′SnH [Ar* = 2,6-Trip2C6H3, where Trip = 2,4,6-triisopropylphenyl; Ar′ = 2,6-Mes2C6H3, where Mes
Publikováno v:
Angewandte Chemie (International ed. in English). 56(8)
A bulky substituted stannane Ar*SnH3 (Ar*=2,6-(2′,4′,6′-triisopropylphenyl)phenyl) was treated with the well-known frustrated Lewis pair (FLP) PtBu3/B(C6F5)3 in varying stoichiometries. To some degree, hydride abstraction and adduct formation i
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 22(22)
Hydrogen can be selectively removed from organotin trihydrides to generate the corresponding organohydrostannylene intermediates. Depending on the size of the substituent and the mode of generation, the intermediates undergo further reactions. Herein