616896-95-8Relevant academic research and scientific papers
Enantioselective Michael additions of β-keto esters to α,β-unsaturated carbonyl compounds catalyzed by a chiral biquinoline N,N′-dioxide-scandium trifluoromethanesulfonate complex
Nakajima, Makoto,Yamamoto, Satoshi,Yamaguchi, Yukiko,Nakamura, Seiichi,Hashimoto, Shunichi
, p. 7307 - 7313 (2003)
A catalytic, enantioselective Michael addition of β-keto esters to α,β-unsaturated carbonyl compounds was achieved by using a chiral biquinoline N,N′-dioxide-scandium trifluoromethanesulfonate complex as a catalyst. The corresponding Michael adducts were
