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Volumn 60, Issue 11, 2003, Pages 2429-2434

Concise synthesis of pyrrolophenanthridine alkaloids using a Pd-catalyzed biaryl coupling reaction with regioselective C-H activation

Author keywords

[No Author keywords available]

Indexed keywords

1 (2 HALOBENZYL) 2,3 DIHYDROINDOLE; ALKALOID DERIVATIVE; ANHYDROLYCORIN 7 ONE; ANHYDROLYCORINE; ASSOANINE; INDOLE DERIVATIVE; LEAD; OXOASSOANINE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; PYRROLOPHENANTHRIDINE ALKALOID; UNCLASSIFIED DRUG;

EID: 0142027269     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-03-9883     Document Type: Article
Times cited : (15)

References (50)
  • 6
    • 77956708370 scopus 로고    scopus 로고
    • ed. by G. A. Cordell, Academic Press, New York
    • a) O. Hoshino, "The Alkaloids" Vol, 51, ed. by G. A. Cordell, Academic Press, New York, 1998, pp. 323-424;
    • (1998) The Alkaloids , vol.51 , pp. 323-424
    • Hoshino, O.1
  • 29
    • 0142060380 scopus 로고    scopus 로고
    • note
    • 7d gave 10 in 79% yield. However, the reaction of 9 under the same conditions gave a mixture of 9 and an unidentified compound.
  • 30
    • 0142123642 scopus 로고    scopus 로고
    • note
    • 5a
  • 31
    • 0000702671 scopus 로고
    • ed. by W. G. Daube, John Wiley & Sons. Inc., New York
    • a) R. F. Heck, Organic Reactions, ed. by W. G. Daube, John Wiley & Sons. Inc., New York, 1982, Vol. 27, pp. 345-390;
    • (1982) Organic Reactions , vol.27 , pp. 345-390
    • Heck, R.F.1
  • 37
    • 0142123640 scopus 로고    scopus 로고
    • note
    • 3) δ=5.25 (2H, s), 6.53 (1H, d, J=3.6), 7.11 (1H, d, J=3.6).
  • 46
    • 0142028325 scopus 로고    scopus 로고
    • note
    • 16b, 16d
  • 47
    • 0142123639 scopus 로고    scopus 로고
    • note
    • The reaction of 16a under an oxygen atmosphere, to accelerate the oxidation, afforded 3 only in 21% yield.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.