A facile synthesis of 7-chloromethyl-1H-indole-2-carboxylates: Replacement of a sulfonic acid functionality by chlorine
Author:
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570420422/fullpdf
Reference23 articles.
1. A facile approach to the synthesis of 5,7-disubstituted indoles via a highly selective lithium–bromine exchange of 5,7-dibromoindoles
2. Directed ortho Metalation Approach to C-7-Substituted Indoles. Suzuki−Miyaura Cross Coupling and the Synthesis of Pyrrolophenanthridone Alkaloids
3. Directed C-7 lithiation of 1-(2,2-diethylbutanoyl)indoles
4. A Concise Synthesis of 7-Substituted Indoles
5. Formamidines in synthesis. An efficient one-pot synthesis of 7-substituted indolines via intramolecular cyclization of (2-phenethyl)formamidines. An asymmetric route to benzopyrrocoline alkaloids
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1. Synthesis of new hexahydro-5H-indolo[3,2-c]acridines and indolylbutanoic acids by Fischer cyclization of arylhydrazones;Chemistry of Heterocyclic Compounds;2018-02
2. The preparation of 5-indolyl-Mannich bases: an expedient source of 5-(chloromethyl)indoles;Tetrahedron Letters;2008-04
3. A facile synthesis of 5(6)‐(chloromethyl)benzimidazoles: Replacement of a sulfonic acid functionality by chlorine;Journal of Heterocyclic Chemistry;2008-03
4. Pyrroles and their Benzo Derivatives: Synthesis;Comprehensive Heterocyclic Chemistry III;2008
5. A facile synthesis of 4-, 6- and 7-formyl-1H-indole-2-carboxylates: The CH2SO3H functionality as a masked formyl group;Journal of Heterocyclic Chemistry;2006-09
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