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Volumn 128, Issue 21, 2006, Pages 6804-6805

Enantioselective organocatalytic aminomethylation of aldehydes: A role for ionic interactions and efficient access to β2-amino acids

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; BETA AMINO ACID; CARBOXYLIC ACID; HYDROGEN; IMINE; ION; PROLINE;

EID: 33744826542     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja061731n     Document Type: Article
Times cited : (162)

References (42)
  • 16
    • 11144333506 scopus 로고    scopus 로고
    • Cordova et al. reported formaldehyde-derived imine generated in situ with aniline derivatives for aminomethylation of ketones catalyzed by proline, but such a strategy is not applicable to aminomethylation of aldehydes. See: (a) Ibrahem, I.; Casas, J.; Cordova, A. Angew. Chem., Int. Ed. 2004, 43, 6528.
    • (2004) Angew. Chem., Int. Ed. , vol.43 , pp. 6528
    • Ibrahem, I.1    Casas, J.2    Cordova, A.3
  • 31
    • 33744814259 scopus 로고    scopus 로고
    • note
    • See Supporting Information for details.
  • 35
    • 0000160925 scopus 로고
    • and ref 7
    • Oxidation of chiral α-substituted aldehydes and alcohols without epimerization: Rangaishenvi, M. V.; Singaram, B.; Brown, H. C. J. Org. Chem. 1991, 56, 3286; and ref 7.
    • (1991) J. Org. Chem. , vol.56 , pp. 3286
    • Rangaishenvi, M.V.1    Singaram, B.2    Brown, H.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.