A Novel Enantioselective Alkylation and Its Application to the Synthesis of an Anticancer Agent

A novel enantioselective alkylation of double benzylic substrates with secondary electrophiles is reported. A simple norephedrine-based chiral ligand was synthesized that gives alkylation product in 95% yield and 95% ee. A unique water effect on the enantioselectivity was unveiled. Good to excellent...

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Veröffentlicht in:Journal of organic chemistry 2003-06, Vol.68 (12), p.4984-4987
Hauptverfasser: Kuo, Shen-Chun, Chen, Frank, Hou, Donald, Kim-Meade, Agnes, Bernard, Charles, Liu, Jinchu, Levy, Stacy, Wu, George G
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Sprache:eng
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Zusammenfassung:A novel enantioselective alkylation of double benzylic substrates with secondary electrophiles is reported. A simple norephedrine-based chiral ligand was synthesized that gives alkylation product in 95% yield and 95% ee. A unique water effect on the enantioselectivity was unveiled. Good to excellent ee values were obtained with a number of double benzylic substrates and secondary electrophiles. This novel reaction has been applied to the synthesis of a promising anticancer agent.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo034380t