期刊
TETRAHEDRON
卷 64, 期 11, 页码 2559-2564出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2008.01.040
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Highly enantioselective arylations of arylaldehydes using arylboronic acids as aryl resource were realized in the presence of a catalytic amount of (2S)-1-ferrocenylmethylaziridin-2-yl(diphenyl)methanol. In addition, the R or S enantiomers of a series of given diarylmethanols can be easily obtained in high yields with excellent enantioselectivities simply by the reverse combinations of both reaction partners. A possible transition state for the catalytic asymmetric addition has been proposed on the basis of previous studies. (c) 2008 Published by Elsevier Ltd.
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