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Synthesis of indolocarbazole quinones; potent aryl hydrocarbon receptor ligands

Bergman, Jan (author)
Karolinska Institutet,Södertörns högskola,Avdelning Naturvetenskap,Karolinska Institute
Wahlström, Niklas (author)
Södertörns högskola,Avdelning Naturvetenskap,Karolinska Institute
Yudina, L N (author)
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Tholander, J (author)
Lidgren, G (author)
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 (creator_code:org_t)
2002
2002
English.
In: Tetrahedron. - 0040-4020 .- 1464-5416. ; 58:7, s. 1443-1452
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Syntheses of indolo[2,3-b]carbazole-6,12-dione and the isomeric indolo[3,2-b]carbazole-6,12-dione, an extremely efficient inducer of the aryl hydrocarbon (Ah) receptor are described. Initial oxidation of the parent indolo[3,2-b]carbazole followed by several different ring-closing strategies produced the latter compound. Entries into syntheses of unsymmetrical 6,12-disubstituted indolo[2,3-b]carbazoles are also described.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

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ref (subject category)
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By the author/editor
Bergman, Jan
Wahlström, Nikla ...
Yudina, L N
Tholander, J
Lidgren, G
About the subject
NATURAL SCIENCES
NATURAL SCIENCES
and Chemical Science ...
Articles in the publication
Tetrahedron
By the university
Södertörn University
Karolinska Institutet

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