메뉴 건너뛰기




Volumn 51, Issue 34, 2010, Pages 4570-4572

Synthesis of lupinacidins A and B via sequential cycloaddition-double elimination

Author keywords

Anthraquinone; Antitumor; Diels Alder reaction; Lupinacidin

Indexed keywords

1,4 CYCLOHEXADIENE; ANTHRAQUINONE DERIVATIVE; ETHYLENE; JUGLONE; LUPINACIDIN A; LUPINACIDIN B; SULFENIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 77955709401     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2010.06.121     Document Type: Article
Times cited : (4)

References (17)
  • 2
    • 77955709051 scopus 로고
    • For synthetic anthraquinones with a benzene ring unit having the same substitution pattern, see
    • For synthetic anthraquinones with a benzene ring unit having the same substitution pattern, see: (a) G. Heller, and P. Lindner Ber. Dtsch. Chem. Ges. 55B 1922 267 269
    • (1922) Ber. Dtsch. Chem. Ges. , vol.55 B , pp. 267-269
    • Heller, G.1    Lindner, P.2
  • 5
    • 0343875362 scopus 로고
    • For examples of naturally occurring bianthraquinones having analogous substitution patterns, see
    • For examples of naturally occurring bianthraquinones having analogous substitution patterns, see: (a) F. Delle Monache, I.L. D'Albuquerque, A. De Andrade Chiappeta, and J.F. De Mello Phytochemistry 31 1992 259 261
    • (1992) Phytochemistry , vol.31 , pp. 259-261
    • Delle Monache, F.1    D'Albuquerque, I.L.2    De Andrade Chiappeta, A.3    De Mello, J.F.4
  • 8
    • 77955716740 scopus 로고    scopus 로고
    • Ref. 2c
    • (d) Ref. 2c.
  • 17
    • 77955717724 scopus 로고    scopus 로고
    • note
    • The chromatographic purification of intermediate 14 was required to obtain 1 in a pure state.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.