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Volumn 49, Issue 46, 2010, Pages 8588-8592

Chiral brønsted acid catalyzed enantioselective α- aminoxylation of enecarbamates

Author keywords

hydroxy ketones; aminoxylation; asymmetric catalysis; Br nsted acid catalysis; nitroso compounds

Indexed keywords

AMINO ALCOHOLS; AMINOXYLATION; AROMATIC KETONES; ASYMMETRIC CATALYSIS; ENANTIOSELECTIVE; NITROSO COMPOUNDS; OXAZOLIDINONES; STEREO-SELECTIVE;

EID: 78049501859     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201002640     Document Type: Article
Times cited : (51)

References (103)
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    • There are scarce examples of linear ketones with almost no N/O selectivity, see
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    • See Ref. [4d]
    • See Ref. [4d].
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    • For details, see the Supporting Information
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    • In all cases, the N-addition products were racemic. For calculation studies, see
    • In all cases, the N-addition products were racemic. For calculation studies, see
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    • The relative configuration was determined by NOE effects as well as by comparison with literature data; see
    • The relative configuration was determined by NOE effects as well as by comparison with literature data; see:, E.-S. Lee, H.-S. Yeom, J.-H. Hwang, S. Shin, Eur. J. Org. Chem. 2007, 3503.
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    • Lee, E.-S.1    Yeom, H.-S.2    Hwang, J.-H.3    Shin, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.