Synthesis of fused indoles from 2,4,6-trinitrotoluene View Full Text


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Article Info

DATE

2003-03

AUTHORS

A. N. Yamskov, A. V. Samet, V. V. Semenov

ABSTRACT

4,6-Dinitro-1-tosylindoline prepared from trinitrotoluene undergoes base-catalyzed condensation with aromatic aldehydes. With salicylaldehyde and 2-hydroxynaphthalene-1-carbaldehyde, the condensation is accompanied by intramolecular nucleophilic substitution for one of the nitro groups to give benzo- and naphthooxepino[4,3,2-cd]indoles, respectively.

PAGES

759-760

Identifiers

URI

http://scigraph.springernature.com/pub.10.1023/a:1023999915911

DOI

http://dx.doi.org/10.1023/a:1023999915911

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1001830316


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