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Volumn , Issue 6, 1998, Pages 590-592

Direct formation of α-dione blocks from o-benzoquinone cycloadditions and their value in the synthesis of fused quinoxalines, 1,10-phenanthrolines and pteridines

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EID: 0003078180     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1998-3135     Document Type: Article
Times cited : (17)

References (45)
  • 40
    • 15844372442 scopus 로고    scopus 로고
    • Benzoquinones have been generated in situ by enzymatic oxidation of catechols and trapped using cycloaddition reactions. Müller, G. H.; Waldman, H. Tetrahedron Lett. 1996, 37, 3833.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3833
    • Müller, G.H.1    Waldman, H.2
  • 41
    • 26844581898 scopus 로고    scopus 로고
    • note
    • 3) δ 1.03 (1H, d, J = 12 Hz); 1.86 (2H, s); 2.42 (2H, s); 2.56 (2H, s); 3.75 (6H, s); 4.23 (2H, t, J = 4 Hz); 6.54 (2H, t, J = 4 Hz); 7.60 (2H, m); 7.94 (2H, m).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.