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Ruthenium-catalyzed asymmetric epoxidation of olefins using H2O2, Part I:: Synthesis of new chiral N,N,N-tridentate pybox and pyboxazine ligands and their ruthenium complexes

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 12, Issue 7, Pages 1855-1874

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.200501261

Keywords

epoxidation; homogeneous catalysis; N ligands; olefins; ruthenium

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The synthesis of chiral tridentate N,N,N-pyridine-2,6-bisoxazolines 3 (pybox ligands) and N,N,N-pyridine-2,6-bisoxazines 4 (pyboxazine ligands) is described in detail. These novel ligands constitute a useful toolbox for the application in asymmetric catalysis. Compounds 3 and 4 are conveniently prepared by cyclization of enantiomerically pure alpha- or beta-amino alcohols with dimethyl pyridine-2,6-dicarboximidate. The corresponding ruthenium complexes are efficient asymmetric epoxidation catalysts and have been prepared in good yield and fully characterized by spectroscopic means. Four of these ruthenium complexes have been characterized by X-ray crystallography. For the first time the molecular structure of a pyboxazine complex {2,6bis-[(4S)-4-phenyl-5,6-dihydro-4H- [1,3] oxazinyl] pyridine} (pyridine-2,6-dicarboxylate) ruthenium (S)-2aa, is presented.

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