Efficient alcoholysis of 5,6-dihydro-1,10-phenanthroline-5,6-epoxide with ytterbium(III) triflate and subsequent enantioselective transesterification with lipases-Reference-Cited by-同舟云学术

Efficient alcoholysis of 5,6-dihydro-1,10-phenanthroline-5,6-epoxide with ytterbium(III) triflate and subsequent enantioselective transesterification with lipases

Published:2009-08 Issue:16 Volume:20 Page:1897-1902
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Schoffers Elke,Kohler Lars

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference26 articles.

1. Advances in Nitrogen Heterocycles;Thummel,2000

2. Reinventing Phenanthroline Ligands − Chiral Derivatives for Asymmetric Catalysis?

3. Chiral pyridine-containing ligands in asymmetric catalysis

4. Preparation of Chiral 5,6-trans-Disubstituted Phenanthrolines from Phenanthroline-5,6-epoxide

5. A Versatile Preparative Route to 5-Substituted-1,10-Phenanthroline Ligands via 1,10-Phenanthroline 5,6-Epoxide

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