Evidence map›Paper›PMID 34128009›Full record

ArticleChemical communications (Cambridge, England)2021

A multicomponent tetrazolo indole synthesis.

Xiaofang Lei, Panagiota Lampiri, Pravin Patil, Giasemi Angeli, Constantinos G Neochoritis, Alexander Dömling

Abstract read
In one paragraph

Article in Chemical communications (Cambridge, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. The Evolution of Fluorescein into A Potential Theranostic Tool.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Highly Stereoselective Ugi/Pictet-Spengler Sequence.The Journal of organic chemistry · 2022
    Article
  8. 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

6 authors.

Xiaofang LeiUniversity of Crete, Department of Chemistry, Heraklion, Greece. kneochor@uoc.gr and University of Groningen, Department of Pharmacy, Drug Design group, Groningen, The Netherlands. a.s.s.domling@rug.nl.
Panagiota LampiriUniversity of Crete, Department of Chemistry, Heraklion, Greece. kneochor@uoc.gr.
Pravin PatilUniversity of Groningen, Department of Pharmacy, Drug Design group, Groningen, The Netherlands. a.s.s.domling@rug.nl.ORCID http://orcid.org/0000-0002-0903-8174
Giasemi AngeliUniversity of Crete, Department of Chemistry, Heraklion, Greece. kneochor@uoc.gr.ORCID http://orcid.org/0000-0002-7111-9899
Constantinos G NeochoritisUniversity of Crete, Department of Chemistry, Heraklion, Greece. kneochor@uoc.gr.ORCID http://orcid.org/0000-0001-5098-5504
Alexander DömlingUniversity of Groningen, Department of Pharmacy, Drug Design group, Groningen, The Netherlands. a.s.s.domling@rug.nl.ORCID http://orcid.org/0000-0002-9923-8873

Funding

Real-time discovery of inhibitors among billion compounds for preview and downloadR01GM097082 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CAMACHO, CARLOS J. · 2011 to 2020
$2.5M
NIGMS NIH HHS R01 GM097082
6 · The paper itself

Abstract

The ubiquitous presence of the indole fragment in natural products and drugs asks for ever novel syntheses. We report an unprecedented mild, two-step synthesis of 2-tetrazolo substituted indoles based on the Ugi-tetrazole reaction combined with an acidic ring closure. A gram-scale synthesis, a bioactive compound and further transformations were performed.

Identifiers

PMID34128009
PMCPMC8259579

What OpenQuestion holds

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Registered trials

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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.