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Volumn , Issue 27, 2010, Pages 5292-5300

Ethyl α-nitrocinnamates in the synthesis of highly functionalized isoxazoles

Author keywords

Alkylation; Michael addition; Multicomponent reactions; Nitrogen heterocycles

Indexed keywords


EID: 77956464573     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201000401     Document Type: Article
Times cited : (41)

References (65)
  • 42
    • 84986477899 scopus 로고
    • Simililar O-alkylation with a nitro group as leaving group has been reported. See: a
    • Simililar O-alkylation with a nitro group as leaving group has been reported. See: a) S. Niwas, S. Kumar, A. P. Bhaduri, Synthesis 1983, 1027-1028;
    • (1983) Synthesis , pp. 1027-1028
    • Niwas, S.1    Kumar, S.2    Bhaduri, A.P.3
  • 47
    • 0038221292 scopus 로고
    • Similar three-membered ring C-alkylation has been reported. See: a
    • Similar three-membered ring C-alkylation has been reported. See: a) N. Ono, T. Yanai, I. Hamamoto, A. Kamimura, A. Kaji, J. Org. Chem. 1985, 50, 2806-2807;
    • (1985) J. Org. Chem. , vol.50 , pp. 2806-2807
    • Ono, N.1    Yanai, T.2    Hamamoto, I.3    Kamimura, A.4    Kaji, A.5
  • 52
    • 77956489777 scopus 로고    scopus 로고
    • -3. CCDC-764659 contains the supplementary crystallographic data for this paper. 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.