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Volumn 53, Issue 26, 2014, Pages 6673-6677

Rhodium-catalyzed asymmetric arylation of β,γ-unsaturated α-ketoamides for the construction of nonracemic γ,γ- diarylcarbonyl compounds

Author keywords

asymmetric synthesis; enantioselectivity; homogeneous catalysis; rhodium; S,P ligands

Indexed keywords

CATALYSIS; ENANTIOSELECTIVITY; LIGANDS; REACTION KINETICS; RHODIUM; UNSATURATED COMPOUNDS;

EID: 84903265429     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201403325     Document Type: Article
Times cited : (43)

References (76)
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    • Recently, a Rh-catalyzed 1,4-addition of arylboronic acid to β,γ-unsaturated α-ketoester was observed to obtain β,β-diaryl-α-ketoester as product in 43% yield and 5%ee. See
    • Recently, a Rh-catalyzed 1,4-addition of arylboronic acid to β,γ-unsaturated α-ketoester was observed to obtain β,β-diaryl-α-ketoester as product in 43% yield and 5%ee. See:, T. S. Zhu, M. H. Xu, Chin. J. Chem. 2013, 31, 321.
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    • The absolute configuration of 3aa was determined by single-crystal X-ray crystallography, displacement ellipsoids set at 50% probability. CCDC995001 (3aa) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • The absolute configuration of 3aa was determined by single-crystal X-ray crystallography, displacement ellipsoids set at 50% probability. CCDC995001 (3aa) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
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    • For solvent effects on the enantioselectivity of the product, see Supporting Information
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    • Bunce, R.A.1    Herron, D.M.2    Johnson, L.B.3    Kotturi, S.V.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.