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A new type of chiral bisoxazoline ligands 1 based on spiro[4,4]-1,6-nonadiene backbone was easily prepared in six steps from racemic spiro[4,4]-nonane-1,6-dione,with the Pd-catalyzed coupling of the enol triflates with CO and amino alcohols as the key steps for the construction of the oxazoline moiety. The structure of the ligand (R,S,S)-1b was unambiguously established by X-ray crystallographic analysis. The chiral Cu(II) complex generated in situ from the combination of spiro bisoxazoline ligand (S,S,S)-1c and Cu(OTf)2 was effective in the catalysis of asymmetric chlorination of the β-ketoester,methyl 1-oxo-2,3-dihydro-1H-indene-2-carboxylate,affording the corresponding chlorinated derivative in 99% yield with 17% ee.
A new type of chiral bisoxazoline ligands 1 based on spiro [4,4] -1,6-nonadiene backbone was easily prepared in six steps from racemic spiro [4,4] -nonane-1,6-dione, with the Pd- catalyzed coupling of the enol triflates with CO and amino alcohols as the key steps for the construction of the oxazoline moiety. The structure of the ligand (R, S, S) -1b was unambiguously established by X-ray crystallographic analysis. The chiral Cu (II) complex generated in situ from the combination of spiro bisoxazoline ligand (S, S, S) -1c and Cu (OTf) 2 was effective in the catalysis of asymmetric chlorination of the β- ketoester, methyl 1- oxo-2, 3-dihydro-1H-indene-2-carboxylate, affording the corresponding chlorinated derivative in 99% yield with 17% ee.