π-Facial selectivities in the coordination of an optically pure fused cyclopentadienyl ligand to arene ruthenium moieties. NMR spectral and structural characterization of a single diastereomer of [(PCp)Ru(Me6C6)]PF6-Reference-Cited by-同舟云学术

π-Facial selectivities in the coordination of an optically pure fused cyclopentadienyl ligand to arene ruthenium moieties. NMR spectral and structural characterization of a single diastereomer of [(PCp)Ru(Me6C6)]PF6

Published:1994-06 Issue:1-2 Volume:221 Page:41-50
ISSN:0020-1693
Container-title:Inorganica Chimica Acta
language:en
Short-container-title:Inorganica Chimica Acta

Author:

Bhaduri Debjani,Nelson John H.,Solujic' Ljiljana,Milosavljevic' Emil B.,Day Catherine L.,Jacobson Robert A.,Gray George A.

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry

Reference30 articles.

1. A designed, enantiomerically pure, fused cyclopentadienyl ligand with C2 symmetry. Synthesis and use in enantioselective titanocene-catalyzed hydrogenations of alkenes

2. Isodicyclopentadienes and related molecules. 38. Homochiral pinene-fused cyclopentadienes. Synthesis and .pi.-facially selective course of Diels-Alder cycloadditions and metallocene formation

3. Synthesis and asymmetric reactivity of enantiomerically pure cyclopentadienylmetal complexes derived from the chiral pool

4. Isodicyclopentadienes and related molecules. 45. (1R)-(-)-Nopol as the source of an optically pure fused cyclopentadienyl ligand. Stereochemical course of complexation to cyclopentadienyltitanium and -zirconium dichloride fragments

5. Isodicyclopentadienes and related molecules. 44. Analysis of the .pi.-facial preference for complexation of a camphor-derived, enantiomerically pure cyclopentadienyl ligand to CpMCl2 fragments (M = Ti and Zr)

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1. Stoichiometric Applications of eta6-Arene Ruthenium(II) Complexes in Organic Chemistry;Current Organic Chemistry;2001-07-01