The First Polymer-Supported and Recyclable Chiral Catalyst for Enantioselective Olefin Metathesis
- 14 February 2002
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 114 (4), 609-613
- https://doi.org/10.1002/1521-3757(20020215)114:4<609::aid-ange609>3.0.co;2-6
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin MetathesisAngewandte Chemie International Edition, 2001
- A Readily Available and User-Friendly Chiral Catalyst for Efficient Enantioselective Olefin MetathesisAngewandte Chemie, 2001
- Catalytic Asymmetric Olefin MetathesisChemistry – A European Journal, 2001
- Tandem Catalytic Asymmetric Ring-Opening Metathesis/Cross MetathesisJournal of the American Chemical Society, 1999
- Superior performance of a chiral catalyst confined within mesoporous silicaChemical Communications, 1999
- Mo-Catalyzed Asymmetric Synthesis of Dihydrofurans. Catalytic Kinetic Resolution and Enantioselective Desymmetrization through Ring-Closing MetathesisJournal of the American Chemical Society, 1998
- Catalytic Asymmetric Addition of ZnPh2 to Ketones: Enantioselective Formation of Quaternary StereocentersJournal of the American Chemical Society, 1998
- Ein molekular definierter, oberflächengebundener Katalysator zur Olefin-Metathese aus Tris(neopentyl)nitridomolybdän(VI)Angewandte Chemie, 1996
- Oxidation of Hindered Phenols. III. The Rearrangement of the 2,6-Di-t-butyl-4-methylphenoxy RadicalJournal of the American Chemical Society, 1955
- Reaction between 2,6-Di-t-butyl-p-cresol and BromineJournal of the American Chemical Society, 1953