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Molecular iodine: An efficient catalyst for the synthesis of both symmetrical and unsymmetrical triindolylmethanes (TRIM)

Paper ID Volume ID Publish Year Pages File Format Full-Text
51925 46858 2008 4 PDF Available
Title
Molecular iodine: An efficient catalyst for the synthesis of both symmetrical and unsymmetrical triindolylmethanes (TRIM)
Abstract

Lewis acid catalyzed synthesis of triindolylmethanes from indole-3-carboxaldehyde and several other indole derivatives is described. A systematic study was carried out to evaluate the catalytic activity of seven Lewis acids and molecular iodine. Iodine appeared to be the most efficient in affording symmetrical and unsymmetrical triindolylmethanes in high yield.

Keywords
Lewis acid; Molecular iodine; Triindolylmethane
First Page Preview
Molecular iodine: An efficient catalyst for the synthesis of both symmetrical and unsymmetrical triindolylmethanes (TRIM)
Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Communications - Volume 9, Issue 7, 1 April 2008, Pages 1681–1684
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis