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Volumn 19, Issue 14, 2009, Pages 3952-3954

Organocatalytic enantioselective hetero-Diels-Alder reaction of aldehydes and o-benzoquinone diimide: Synthesis of optically active hydroquinoxalines

Author keywords

Aldehydes; Chiral hydroquinoxalines; Hetero Diels Alder reaction; Inverse electron demand; o Benzoquinone diimide

Indexed keywords

ALDEHYDE DERIVATIVE; AMINE; BENZOQUINONE DERIVATIVE; IMIDE; QUINOXALINE DERIVATIVE;

EID: 67649975255     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.03.013     Document Type: Article
Times cited : (40)

References (28)
  • 8
    • 67649987882 scopus 로고    scopus 로고
    • U.S. Patent Appl. 20050020591
    • Su, D. -S.; Bock, M. G. U.S. Patent Appl. 20050020591, 2005.
    • (2005)
    • Su, D.-S.1    Bock, M.G.2
  • 19
    • 0344835672 scopus 로고    scopus 로고
    • For inverse electron demand HDAR by amino-catalysis, see:
    • For inverse electron demand HDAR by amino-catalysis, see:. Juhl K., and Jørgensen K.A. Angew. Chem., Int. Ed. 42 (2003) 1498-1501
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 1498-1501
    • Juhl, K.1    Jørgensen, K.A.2
  • 25
    • 67649950487 scopus 로고    scopus 로고
    • note
    • Slow decomposition of 4a was detected in the NMR analysis in a chloroform solution probably due to a slightly acidic condition.
  • 27
    • 67649959976 scopus 로고    scopus 로고
    • note
    • The relative configuration of compounds 9 and 10 was determined by NOE analysis.
  • 28
    • 67649963156 scopus 로고    scopus 로고
    • A plausible catalytic mechanism has been proposed, please see Supplementary data
    • A plausible catalytic mechanism has been proposed, please see Supplementary data.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.