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Synfacts 2007(1): 0054-0054
DOI: 10.1055/s-2006-955722
DOI: 10.1055/s-2006-955722
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York
New Ligands: Hydroxyoxazolinyl[2.2]paracyclophanes in Asymmetric Catalysis
C. Bolm*, D. K. Whelligan
RWTH Aachen, Germany
Further Information
Publication History
Publication Date:
15 December 2006 (online)

Significance
Synthesis and use of pseudo-geminal, pseudo-ortho and ortho hydroxyoxazolinyl[2.2]paracyclophanes as N,O-ligands is described. The pseudo-geminal compounds were accessed by directed bromination followed by lithiation and B(OMe)3 quench. Oxidation with H2O2 gave the desired ligands 1a and 1b. The pseudo-ortho ligand was accessed in a similar manner, except conversion into the benzyl ethers, separation, and subsequent deprotection was necessary to give 2a and 2b. The ortho ligand was prepared as previously described by the same authors ( J. Org. Chem. 2006, 71, 4609-4618).