Literature DB >> 31481819

Friedel-Crafts Alkylation of Indoles with Trichloroacetimidates.

Tamie Suzuki1, John D Chisholm1.   

Abstract

Substituted indole scaffolds are often utilized in medicinal chemistry as they regularly possess significant pharmacological activity. Therefore the development of simple, inexpensive and efficient methods for alkylating the indole heterocycle continues to be an active research area. Reported are reactions of trichloroacetimidate electrophiles and indoles to address the challenges of accessing alkyl decorated indole structures. These alkylations perform best when either the indole or the imidate is functionalized with electron withdrawing groups to avoid polyalkylation.

Entities:  

Keywords:  Alkylation; Friedel-Crafts; Indole; Lewis Acid

Year:  2019        PMID: 31481819      PMCID: PMC6720118          DOI: 10.1016/j.tetlet.2019.04.007

Source DB:  PubMed          Journal:  Tetrahedron Lett        ISSN: 0040-4039            Impact factor:   2.415


  43 in total

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2.  Formation of Pyrroloindolines via the Alkylation of Tryptamines with Trichloroacetimidates.

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