SYNTHESIS OF ACTIVATED 3-ARYLINDOLES

A wide range of substituted 3-aryl-4,6-dimethoxyindoles (6) has been synthesized from the related alpha-anilinoacetophenones (5), in which the nitrogen atom is protected by a trifluoroacetyl or acetyl group. This method has led to the synthesis of a 3,7'-biindolyl (12).

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Bibliographic Details
Published inAustralian journal of chemistry Vol. 47; no. 9; pp. 1741 - 1750
Main Authors BLACK, DS, BOWYER, MC, BOWYER, PK, IVORY, AJ, KIM, M, KUMAR, N, MCCONNELL, DB, POPIOLEK, M
Format Journal Article
LanguageEnglish
Published COLLINGWOOD C S I R O PUBLICATIONS 01.01.1994
Subjects
Chemistry
Chemistry, Multidisciplinary
Physical Sciences
Science & Technology
POLYINDOLENINE ALKALOIDS
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Summary:A wide range of substituted 3-aryl-4,6-dimethoxyindoles (6) has been synthesized from the related alpha-anilinoacetophenones (5), in which the nitrogen atom is protected by a trifluoroacetyl or acetyl group. This method has led to the synthesis of a 3,7'-biindolyl (12).
ISSN:0004-9425
DOI:10.1071/CH9941741