High Enantioselection in the Rearrangement of Allylic Imidates with Ferrocenyl Oxazoline Catalysts
- 1 March 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 121 (12) , 2933-2934
- https://doi.org/10.1021/ja983263q
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Planar-chiral cyclopalladated ferrocenyl amines and imines as enantioselective catalysts for allylic imidate rearrangementsTetrahedron: Asymmetry, 1998
- Asymmetric aza-Claisen rearrangement of allyl imidates catalyzed by homochiral cationic palladium(II) complexesTetrahedron: Asymmetry, 1998
- Cyclopalladated ferrocenyl amines as enantioselective catalysts for the rearrangement of allylic imidates to allylic amidesTetrahedron Letters, 1997
- Cyclopropanation with Diazomethane and Bis(oxazoline)palladium(II) ComplexesThe Journal of Organic Chemistry, 1997
- First Enantioselective Catalyst for the Rearrangement of Allylic Imidates to Allylic AmidesThe Journal of Organic Chemistry, 1997
- Highly Diastereoselective Ortho Lithiations of Chiral Oxazoline-Substituted FerrocenesThe Journal of Organic Chemistry, 1995
- Oxidative cleavage of mono-, di-, and trisubstituted olefins to methyl esters through ozonolysis in methanolic sodium hydroxideThe Journal of Organic Chemistry, 1993
- A convenient method for the preparation of monolithioferroceneTetrahedron Letters, 1990
- Mercury(II)‐ and Palladium(II)‐Catalyzed [3,3]‐Sigmatropic Rearrangements [New Synthetic Methods (46)]Angewandte Chemie International Edition in English, 1984
- Oxidative N-dearylation of 2-azetidinones. p-Anisidine as a source of azetidinone nitrogenThe Journal of Organic Chemistry, 1982