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s Synthesis of bis(indolyl)methanes Catalyzed by Triethylborane
- Source: Letters in Organic Chemistry, Volume 12, Issue 5, Jan 2015, p. 332 - 336
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- 01 Jan 2015
Abstract
Triethylborane (TEB) was found to be a mild, efficient, and acid catalyst in electrophilic substitution reaction of indoles with aldehydes compounds to afford the corresponding bis(indolyl)methanes. Vibrindole A (5) and bis(indolyl)methanes derivatives 16 and 18 were synthesized using this methodology. Compound 16 is an intermediary in the synthesis of the natural bisindoles arsindoline B (2) and streptindole (6). The structure of vibrindole A (5) was unequivocally confirmed by a single crystal X-ray diffraction analysis.
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