Evidence map›Paper›PMID 31481819›Full record

ArticleTetrahedron letters2019

Friedel-Crafts Alkylation of Indoles with Trichloroacetimidates.

Tamie Suzuki, John D Chisholm

Abstract read
In one paragraph

Article in Tetrahedron letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Formation of PyrroloindolinesTetrahedron letters · 2021
    Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Tamie SuzukiDepartment of Chemistry, 1-014 Center for Science and Technology, Syracuse University, Syracuse, NY 13244.
John D ChisholmDepartment of Chemistry, 1-014 Center for Science and Technology, Syracuse University, Syracuse, NY 13244.

Funding

New Methods for the Synthesis of PyrroloindolinesR15GM116054 · NIGMS · SYRACUSE UNIVERSITY · PI CHISHOLM, JOHN DANIEL · 2015 to 2015
$318k
NIGMS NIH HHS R15 GM116054
6 · The paper itself

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.

Indexed as

AlkylationFriedel-CraftsIndoleLewis Acid

Identifiers

PMID31481819
PMCPMC6720118

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.