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pro vyhledávání: '"Patrick Liptau"'
Publikováno v:
Dalton Trans.. :1409-1415
Treatment of acetonitrile (1 equiv.) with n-butyllithium (0.95 equiv.) followed by chlorodiphenylphosphine (0.95 equiv.) under optimised reaction conditions gave a ca. 60% yield of bis(diphenylphosphino)acetonitrile (dppmCN, 1). The bidentate ligand
Autor:
Roland Fröhlich, Gerhard Erker, Frank Hollmann, Gerald Kehr, Ludger Tebben, Bernhard Rieger, Patrick Liptau
Publikováno v:
European Journal of Organic Chemistry. 2005:1909-1918
An intramolecular Mannich reaction (HNMe2, TiCl4) was used to convert 1,1'-diacetylferrocene to the unsaturated amino[3]ferrocenophane 2. Subsequent hydrogenation gave 3. To obtain enantiomerically pure chelate P,P-[3]ferrocenophane ligands the readi
Publikováno v:
Organometallics. 23:21-25
Treatment of the dimethylamino-[3]ferrocenophane 1a with B(C6F5)3 results in hydride abstraction at the −CH(NMe2) moiety in α-position to the ferrocene nucleus to yield the corresponding cation 4a....
Publikováno v:
European Journal of Inorganic Chemistry. 2003:3590-3600
Treatment of 1,1′-diacetylferrocene (4) with dimethylamine and TiCl4 yielded the unsaturated dimethylamino-substituted [3]ferrocenophane product 5. Its catalytic hydrogenation gave the corresponding saturated [3]ferrocenophane system 6 (trans/cis
Autor:
Gerald Kehr, Stefan Grimme, Takashi Seki, Roland Fröhlich, Alexandra Abele, Gerhard Erker, Patrick Liptau
Publikováno v:
Organometallics. 22:2226-2232
Treatment of 1,1‘-diacetylferrocene (1) with dimethylamine, catalyzed by titanium tetrachloride, proceeded in a Mannich-type C−C coupling reaction to yield the unsaturated [3]ferrocenophane 2. Subs...
Publikováno v:
Journal of Organometallic Chemistry. :621-630
Treatment of lithium(1-dimethylamino-ethenyl)cyclopentadienide (5a) with FeCl2 generated the corresponding substituted ferrocene (2a) that rapidly underwent cyclization in a subsequent Mannich-type condensation reaction to yield the unsaturated dimet
Publikováno v:
Acta Crystallographica Section C Crystal Structure Communications. 56:e390-e391
In the title compound, [Cr(C13H11N)(CO)5], the imino ligand displays weak π-acceptor capabilities and, in contrast to Fischer-type carbene complexes, is not positioned on the bisecting line of the angle between two CO ligands.
Autor:
Patrick Liptau, Ludger Tebben, Gerald Kehr, Roland Frhlich, Gerhard Erker, Frank Hollmann, Bernhard Rieger
Publikováno v:
European Journal of Organic Chemistry; May2005, Vol. 2005 Issue 9, p1909-1918, 10p
Publikováno v:
European Journal of Inorganic Chemistry; Dec2004, Vol. 2004 Issue 23, p4586-4590, 5p
Publikováno v:
European Journal of Inorganic Chemistry; Oct2003, Vol. 2003 Issue 19, p3590, 11p