Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Walter Weissensteiner"'
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 12, Pp m1806-m1807 (2011)
The title structure, [Fe2(C5H5)2(C14H19BBrN)], contains a chiral and asymmetrically 2,2′′-disubstituted biferrocene designed as precursor for enantioselective non-C2-symmetric biferrocenyldiphosphine catalysts. The mean bond lengths in the biferr
Externí odkaz:
https://doaj.org/article/e7c8397e27ed46d3984c5c71e6c833f7
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 10, Pp m1377-m1378 (2011)
The racemic title compound, [FePdCl2(C5H5)(C36H29P2)]·2(CH3)2SO, features a Pd-chelating 1,3-diphosphine, which is substituted at a P-bearing asymmetric C atom by a ferrocenyl group. The PdII atom is in a distorted quadratic coordination by two P an
Externí odkaz:
https://doaj.org/article/d54828fda1414810aedd1ec2a7f3b6d5
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 10, Pp m1379-m1380 (2011)
The asymmetric unit of the title compound, [FeRuCl(C5H5)(C10H14)(C37H31P2)]PF6, contains two independent, geometrically similar RuII complexes of a chiral ferrocenyldiphosphane with piano-stool coordination through the η6-bound p-cymene ligand, two
Externí odkaz:
https://doaj.org/article/915b81450bed4e69804adc5a72d471b6
Publikováno v:
CHIMIA, Vol 55, Iss 9 (2001)
Novel enantiopure ferrocene-based aminophosphine and diphosphine ligands for asymmetric catalysts have been developed. In all cases a highly flexible synthetic approach allowed access to ligands with different ferrocenyl backbones and with a variety
Externí odkaz:
https://doaj.org/article/9873a34ae7124f5cbc8ad950abe7559f
Publikováno v:
Journal of Organometallic Chemistry. 716:32-38
Negishi coupling conditions were identified that allowed the synthesis of unsymmetrically 2,2″-disubstituted biferrocenes from non-identical ferrocene fragments. The coupling reaction of (R)-1-(N,N-dimethylamino)ethylferrocene (1) with enantiopure
Autor:
Afrooz Zirakzadeh, Walter Weissensteiner, Raffael Schuecker, Felix Spindler, Kurt Mereiter, Nikolaus Gorgas
Publikováno v:
Organometallics. 31:4241-4250
Three novel routes have been developed for the synthesis of ferrocenyl-based phosphino-oxazolines in which the phosphino unit is attached to a ferrocenylmethyl or a ferrocenylethyl side chain. In t...
Publikováno v:
Synthesis. 2012:265-271
A catalytic asymmetric cycloaddition reaction of fluoromethyl-substituted nitroalkenes with azomethine ylides was developed using a catalyst derived from copper(I) perchlorate and a commercially available, chiral Walphos ligand. This method provides
Publikováno v:
Organometallics. 30:4711-4719
A highly flexible and modular synthesis of 15 chiral nonracemic ferrocenyloxazolines—all based on a ferrocenylethyl backbone—is described. Starting from N,N-dimethylaminoethyl ferrocene a range of ...
Autor:
M. Carmen Carrión, Javier Rodríguez Torres, Afrooz Zirakzadeh, Blanca R. Manzano, M. Angeles de la Peña, A. E. Mucientes, Francisco Sepúlveda, Félix A. Jalón, Ana M. Rodríguez, Walter Weissensteiner
Publikováno v:
Organometallics. 30:3490-3503
Several ferrocene-based chiral nonracemic aminophosphine and racemic hydroxyphosphine ligands have been used in the synthesis of RuII(arene) derivatives (arene = p-cymene, benzene). The reaction of suitable ruthenium complexes with the aminophosphine
Publikováno v:
Organometallics. 29:6443-6458
The stereochemical course of the exchange reaction of α-methoxy or α-dimethylamino groups by phosphines in acetic acid has been studied for ferrocene derivatives that have either a ferrocenylethyl ...