Synthesis of 2,2'-biindolyls; Potential intermediates for indolocarbazole alkaloids

Article abstract of DOI:10.1080/00397919408010172

The synthesis of 2,2'-biindolyls oxygenated in the benzenoid ring is reported. Wittig-Horner reaction of the phosphonate esters of 1- benzenesulfonyl-2-bromomethyl-3-substituted indoles with o- nitrobenzaldehydes followed by deoxygenation with triethyl phosphite gave 2,2'-biindolyls.

Full text of DOI:10.1080/00397919408010172

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Synthetic Communications: An
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Organic Chemistry
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Synthesis of 2,2′-Biindolyls;
Potential Intermediates for
Indolocarbazole Alkaloids
K. Jesudoss a & P. C. Srinivasan a
a Department of Organic Chemistry , University of
Madras , Guindy Campus, Madras, 600 025, India
Published online: 23 Sep 2006.
To cite this article: K. Jesudoss & P. C. Srinivasan (1994) Synthesis of 2,2′-Biindolyls;
Potential Intermediates for Indolocarbazole Alkaloids, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 24:12,
1701-1708, DOI: 10.1080/00397919408010172
To link to this article: http://dx.doi.org/10.1080/00397919408010172
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