Ring D modifications of ellipticine. Part 2. Chlorination of ellipticine via its N-oxide and synthesis and selective acetylation of 5,6,11-trimethyl-5H-benzo[b]carbazole.

Tetrahedron

Volumn 50, Issue 16, 1994, Pages 4811-4828

  Boogaard, Adrian T ^a   Pandit, Upendra K ^a   Koomen, Gerrit Jan ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

2 ACETYL 5,6,11 TRIMETHYL 5H BENZO[B]CARBAZOLE; 3 CHLOROELLIPTICINE; 5,6,11 TRIMETHYL 5H BENZO[B]CARBAZOLE; ELLIPTICINE DERIVATIVE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTINEOPLASTIC ACTIVITY; ARTICLE; CONTROLLED STUDY; DRUG SYNTHESIS; HUMAN; HUMAN CELL; LEUKEMIA L 1210; MOUSE; NONHUMAN; PRIORITY JOURNAL; REACTION ANALYSIS; TUMOR CELL;

EID: 0028225038     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)85018-3     Document Type: Article

References (47)

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2. Ellipticine
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5. Approaches to the Synthesis of the Antitumor Pyridocarbazole Alkaloids
6. Synthesis of isoquinolines from indenes
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9. Aromatic Keton Syntesis
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11. �ber eine neue Isochinolinsynthese
12. Persulphate oxidations. Part XI. Oxidative dimerisation of aminonaphthoquinones