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Volumn 130, Issue 24, 2008, Pages 7556-7557

Asymmetrie imino aza-enamine reaction catalyzed by axially chiral dicarboxylic acid: Use of arylaldehyde N,N-dialkylnydrazones as acyl anion equivalent

Author keywords

[No Author keywords available]

Indexed keywords

ANION; DICARBOXYLIC ACID; ENAMINE; HYDRAZONE DERIVATIVE;

EID: 45249095786     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja802704j     Document Type: Article
Times cited : (85)

References (23)
  • 12
    • 38349189109 scopus 로고    scopus 로고
    • For a recent review on chiral Brønsted acid catalysis, see
    • For a recent review on chiral Brønsted acid catalysis, see: Akiyama, T. Chem. Rev. 2007, 107, 5744.
    • (2007) Chem. Rev , vol.107 , pp. 5744
    • Akiyama, T.1
  • 16
    • 9444255109 scopus 로고    scopus 로고
    • For the use of acylsilanes, see: a
    • For the use of acylsilanes, see: (a) Mattson, A. E.; Scheidt, K. A. Org. Lett. 2004, 6, 4363.
    • (2004) Org. Lett , vol.6 , pp. 4363
    • Mattson, A.E.1    Scheidt, K.A.2
  • 21
    • 32344453167 scopus 로고    scopus 로고
    • For the other examples using formaldehyde N,N-dialkylhydrazones in organocatalysis, see: (a) Pettersen, D.; Herrera, R. P.; Bernardi, L.; Fini, F.; Sgarzani, V.; Fernandez, R.; Lassaletta, J. M.; Ricci, A. Synlett 2006, 239.
    • For the other examples using formaldehyde N,N-dialkylhydrazones in organocatalysis, see: (a) Pettersen, D.; Herrera, R. P.; Bernardi, L.; Fini, F.; Sgarzani, V.; Fernandez, R.; Lassaletta, J. M.; Ricci, A. Synlett 2006, 239.
  • 23
    • 45249083749 scopus 로고    scopus 로고
    • Isolated as an equilibrating mixture of two isomers (∼3:1 ratio). For details, see Supporting Information.
    • Isolated as an equilibrating mixture of two isomers (∼3:1 ratio). For details, see Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.