Synthesis of a bis-pyrrolo-quinone structure analogue to wakayin

Tetrahedron Letters

Volumn 40, Issue 20, 1999, Pages 3889-3890

  Barret, Roland ^a   Roue, Nathalie ^b,c  

^a UNIVERSITÉ LYON 1   (France)

^b UNIVERSITÉ DE REIMS CHAMPAGNE ARDENNE   (France)

^c KAROLINSKA INSTITUTE   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

1,4 BENZOQUINONE DERIVATIVE; BISPYRROLOQUINONE; ETHYLAMINE; UNCLASSIFIED DRUG; WAKAYIN;

ARTICLE; ASCIDIACEA; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; ENZYME INHIBITION; SYNTHESIS;

EID: 0033553368     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00640-1     Document Type: Article

References (9)

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3. 3-Zhang L.; Cava, M. P.; Rogers, R. D.; Rogers, L. M. Tetrahedron Lett., 1998, 39, 7677.
4. 4-Barret, R.; Roue, N.; Fillion, H. Chem. Pharm. Bull., 1998, 46, 548.
5. 5-5 was synthesized from 4,7-dimethoxyindole (see: Showalter, H. D. H.; Pohlmann, G. Org. Proc. Intern., 1992, 24, 484); 4,7-dimethoxyindole was sulfonylated and then oxidized by using CAN.
6. 6-Jackson, Y. A.; Billimoria, A. D.; Sadanandan, E. V.; Cava, M. P. J. Org. Chem., 1995, 60, 3543.
7. 7-Edstrom, E. D.; Jones, Z. Tetrahedron Lett., 1995, 36, 7039.
8. 8-Oikawa, Y.; Yoshida, T.; Mohri, K.; Yonemistu, O. Heterocycles, 1979, 12, 1457.
9. 3OD) δ (ppm): 179.7, 173.4, 138.0, 137.6, 134.8, 134.7, 129.3, 126.1, 126.0, 125.9, 124.0, 123.1, 122.3, 121.3, 117.1, 112.4, 108.3.