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Volumn 7, Issue 5, 2009, Pages 860-862

Synthesis of the pyrrolo[2,3-c]carbazole core of the dictyodendrins

Author keywords

[No Author keywords available]

Indexed keywords

MARINE ALKALOIDS; SUZUKI CROSS-COUPLING REACTIONS;

EID: 60749134373     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b822933n     Document Type: Article
Times cited : (41)

References (19)
  • 11
    • 33751554339 scopus 로고
    • Pyrrole boronic ester 5 was reacted with p-bromoanisole without previous purification. Note: when 5 was isolated and purified, it was obtained in very low yield (24%) The N-alkylation methodology used was the same as that developed by Fürstner et al. in the synthesis of storniamide A:
    • B. L. Bray P. H. Mathies R. Naef D. R. Solas T. T. Tidwell D. R. Artis J. M. Muchowski J. Org. Chem. 1990 55 6317
    • (1990) J. Org. Chem. , vol.55 , pp. 6317
    • Bray, B.L.1    Mathies, P.H.2    Naef, R.3    Solas, D.R.4    Tidwell, T.T.5    Artis, D.R.6    Muchowski, J.M.7
  • 15
    • 33746628876 scopus 로고    scopus 로고
    • The stereochemistry of (Z)- 15 was confirmed by a nOe effect between indole proton H3 and the enol ether proton COSY correlation was observed between NH and indole proton H3 -6427
    • J. S. Bajwa G.-P. Chen K. Prasad O. Repi T. J. Blacklock Tetrahedron. Lett. 2006 47 6425 6427
    • (2006) Tetrahedron. Lett. , vol.47 , pp. 6425
    • Bajwa, J.S.1    Chen, G.-P.2    Prasad, K.3    Repi, O.4    Blacklock, T.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.