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Volumn 59, Issue 37, 2003, Pages 7307-7313

Enantioselective Michael additions of β-keto esters to α,β-unsaturated carbonyl compounds catalyzed by a chiral biquinoline N,N′-dioxide-scandium trifluoromethanesulfonate complex

Author keywords

Catalyst; Chiral biquinoline; Enantioselection; Enantioselectivities; Michael addition; N oxide; Scandium trifluoromethanesulfonate; , unsaturated carbonyl compounds

Indexed keywords

CARBONYL DERIVATIVE; SULFONIC ACID DERIVATIVE;

EID: 0042884007     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(03)01139-6     Document Type: Article
Times cited : (74)

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    • For the reaction of tert-butyl ester 2e, a lower concentration resulted in a slightly better enantioselectivity (0.5 mM: 88% yield, 80% ee, 0.1 mM: 89% yield, 84% ee).
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