期刊
ISRAEL JOURNAL OF CHEMISTRY
卷 41, 期 4, 页码 247-249出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1560/6GRQ-YRVV-6KU3-RHGX
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Asymmetric Michael reactions of beta-ketoesters with enones were effectively catalyzed by complexes of silver salts and BINAP derivatives in water. The reactions have proved to give Michael adducts in high yields with high enantioselectivities. These reactions are the first example of Lewis acid-catalyzed asymmetric Michael reactions in water.
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