4.0 Article

Chiral ytterbium silylamide catalyzed enantioselective phospha-Michael addition of diethyl phosphite to chalcones

Journal

TETRAHEDRON-ASYMMETRY
Volume 25, Issue 13-14, Pages 989-996

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2014.06.008

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Funding

  1. National Natural Science Foundation of China [21272168, 20872106]

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An efficient and enantioselective phospha-Michael addition of diethyl phosphite to chalcones has been established. In the presence of a catalytic amount of chiral lanthanide silylamide generated from [(Me3Si)(2)N](3)Yb(mu-Cl)Li(THF)(3) and salen, the reaction produced the target gamma-oxophosphonates with high yields and enantioselectivity. (C) 2014 Elsevier Ltd. All rights reserved.

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