Brunner, Henri and Weber, Matthias and Zabel, Manfred (2003) Asymmetric catalysis, 154. New 1,1 '-binaphthyl ligands for enantioselective catalysis. ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, 58 (9). pp. 821-826. ISSN 0932-0776
Full text not available from this repository. (Request a copy)Abstract
Chiral binaphthyl compounds, especially those with different substituents in 2- and 2'-position of the binaphthyl system, have gained interest as constituents of successful ligands in various catalytic reactions. Here, we present the synthesis and characterization of new binaphthyl ligands containing oxazoline, cyano and amide substituents in 2'-position in addition to methoxy, hydroxy or amino groups in 2-position. Starting from these compounds new ligands for enantioselective catalysis will be accessible.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | SUBSTITUTION; DERIVATIVES; NITRILES; ALCOHOLS; NOBIN; binaphthyl derivatives; chirality; X-ray structure |
| Subjects: | 500 Science > 540 Chemistry & allied sciences |
| Divisions: | Chemistry and Pharmacy > Institut für Anorganische Chemie > Alumni or Retired Professors > Prof. Dr. Henri Brunner |
| Depositing User: | Dr. Gernot Deinzer |
| Date Deposited: | 04 Aug 2021 11:29 |
| Last Modified: | 04 Aug 2021 11:29 |
| URI: | https://pred.uni-regensburg.de/id/eprint/38712 |
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