Asymmetric Catalysis of the Diels−Alder Reaction Using Dicationic Zirconocene Complexes
- 16 February 2000
- journal article
- Published by American Chemical Society (ACS) in Organometallics
- Vol. 19 (6) , 947-949
- https://doi.org/10.1021/om990759n
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Mukaiyama Aldol Reactions Catalyzed by Zirconocene Bis(triflate) Complexes: Stereochemistry and Mechanisms for C−C Bond FormationThe Journal of Organic Chemistry, 1998
- Diels−Alder Reactions of Oxazolidinone Dienophiles Catalyzed by Zirconocene Bis(triflate) Catalysts: Mechanism for Asymmetric InductionOrganometallics, 1998
- Improved Procedure for the Preparation of Enantiomerically Pure Ethylenebis(tetrahydroindenyl)zirconium DerivativesThe Journal of Organic Chemistry, 1997
- Enantioselective C-C and C-H Bond Formation Mediated or Catalyzed by Chiral ebthi Complexes of Titanium and ZirconiumAngewandte Chemie International Edition in English, 1996
- Homogeneous Catalysis. Mechanisms of the Catalytic Mukaiyama Aldol and Sakurai Allylation ReactionsJournal of the American Chemical Society, 1995
- Asymmetric Induction in the Diels-Alder Reaction Catalyzed by Chiral Metallocene Triflate Complexes: Dramatic Effect of Solvent PolarityOrganometallics, 1995
- Use of organometallic complexes of ruthenium in the Lewis acid catalyzed hetero Diels-Alder reactionTetrahedron Letters, 1989
- Synthesis and chemistry of [Cp2Zr(CH3CN)3][BPh4]2: a five-coordinate, dicationic zirconocene complexInorganic Chemistry, 1987