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Volumn 15, Issue 46, 2009, Pages 12819-12827

Kinetic resolution of aminoalkenes by asymmetric hydroamination: A mechanistic study

Author keywords

Asymmetric catalysis; Hydroamination; Kinetic resolution; Rare earths; Reaction mechanisms

Indexed keywords

ALIPHATIC SUBSTITUENTS; AMINO GROUP; AROMATIC SYSTEM; ARYL SUBSTITUENTS; ASYMMETRIC CATALYSIS; CATALYST PAIR; CYCLIZATION RATES; DIASTEREO-SELECTIVITY; DIASTEREOMERIC; ENANTIOPURE; HIGH EFFICIENCY; HYDROAMINATIONS; KINETIC RESOLUTION; KINETIC STUDY; MECHANISTIC STUDIES; METAL CENTERS; METHOXYMETHYL; PHENYL SUBSTITUENTS; REACTION MECHANISM; RELATIVE RATES; RESOLUTION PROCESS; STEREOCENTERS;

EID: 71549165768     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200902229     Document Type: Article
Times cited : (54)

References (143)
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    • The (dynamic) kinetic resolution of racemic amines can be effected by using various enzymatic methodologies; for selected examples, see: a) F. van Rantwijk, R. A. Sheldon, Tetrahedron 2004, 60, 501;
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    • note
    • slow for all substrates. Note, however, that for substrate 3 e the S enantiomer is the faster reacting enantiomer when using the (R)-binaphtholate catalysts.
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    • note
    • 19F NMR spectroscopic chemical shift of the Mosher amide of 3 g obtained in the fractional crystallization is in agreement with this assignment.
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    • CCDC-739753 contains the supplementary crystallographic data for the (R)-Mosher amide of (S)-5. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre
    • CCDC-739753 contains the supplementary crystallographic data for the (R)-Mosher amide of (S)-5. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.