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Volumn , Issue 24, 2006, Pages 2586-2588

Regioselective photo-oxidation of 1-benzyl-4,9-dihydro-3H-β-carbolines

Author keywords

[No Author keywords available]

Indexed keywords

BETA CARBOLINE; NATURAL PRODUCT;

EID: 33745224995     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b604922b     Document Type: Article
Times cited : (30)

References (15)
  • 7
    • 0030757383 scopus 로고    scopus 로고
    • This observation is not new, since related compounds of type 5/6 have been isolated after basic work-up of the Bischler-Napieralski reaction and it has been linked to the spontaneous oxidation of an initially formed 4-type compound;
    • O. L. Radchenko V. L. Novikov G. B. Elyakov Tetrahedron Lett. 1997 38 5339
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5339
    • Radchenko, O.L.1    Novikov, V.L.2    Elyakov, G.B.3
  • 13
    • 33745204988 scopus 로고    scopus 로고
    • 7 who proposed a similar mechanism in a related isoquinoline case. The alternative concerted ene mechanism was discounted on the basis of structure-activity studies
    • 7 who proposed a similar mechanism in a related isoquinoline case. The alternative concerted ene mechanism was discounted on the basis of structure-activity studies
  • 14
    • 13844283656 scopus 로고
    • That is in agreement with the known fact that the natural product xestomanzamine B was gradually converted (at 21°C, for 20 days) presumably via air-oxidation to xestomanzamine A.
    • G. Cauzzo G. Jori J. Org. Chem. 1972 37 1429
    • (1972) J. Org. Chem. , vol.37 , pp. 1429
    • Cauzzo, G.1    Jori, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.