Chiral Metallocenes. 3.1 The Enantioselective Reduction of CX Bonds (X = O or CH2) by the Chiral ansa-Metallocenes (R)- or (S)-[TiCl2(η5:η5- C5Me4SiMe2C5H3R*)] (R* = Menthyl or Neomenthyl)
Author:
Affiliation:
1. Department of Chemistry, University of Sheffield, Sheffield S3 7HF, England
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om020618c
Reference60 articles.
1. Chiral sandwich compounds of ruthenium(II) and (IV): X-ray crystal structure of [Ru{η5-C5H4(neomenthyl)}2I]I3
2. Chiral metallocenes: the synthesis and X-ray crystal structures of TiCl2η5:η5-C5Me4SiMe2C5H3R*) (R* = menthyl or neomenthyl) and related compounds
3. Chiral Organolanthanides Designed for Asymmetric Catalysis. A Kinetic and Mechanistic Study of Enantioselective Olefin Hydroamination/Cyclization and Hydrogenation by C1-Symmetric Me2Si(Me4C5)(C5H3R*)Ln Complexes where R* = Chiral Auxiliary
4. Chiral organolanthanide complexes for enantioselective olefin hydrogenation
5. Highly Enantioselective Hydrogenation of Cyclic Enol Acetates Catalyzed by a Rh-PennPhos Complex
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