Evidence map›Paper›PMID 21350743›Full record

ArticleChemical communications (Cambridge, England)2011

Functionalization of the corrole ring: the role of isocorrole intermediates.

Luca Tortora, Sara Nardis, Frank R Fronczek, Kevin M Smith, Roberto Paolesse

Abstract read
In one paragraph

Article in Chemical communications (Cambridge, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. β-Nitro-5,10,15-tritolylcorroles.Inorganic chemistry · 2012
    Article
  6. Article
  7. Synthetic protocols for the nitration of corroles.Journal of porphyrins and phthalocyanines · 2011
    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

5 authors.

Luca TortoraDipartimento di Scienze e Tecnologie Chimiche, Università di Roma Tor Vergata, via della Ricerca Scientifica 1, 00133 Rome, Italy.
Sara Nardis
Frank R Fronczek
Kevin M Smith
Roberto Paolesse

Funding

SYNTHESES AND CELLULAR STUDIES OF NEW PHOTOSENSITIZERS FOR MEDICAL APPLICATIONSR01CA132861 · NCI · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI SMITH, KEVIN M · 2009 to 2013
$1.5M
NCI NIH HHS CA 132861NCI NIH HHS R01 CA132861
6 · The paper itself

Abstract

Bromination of 3-nitro-5,10,15-triarylcorrole selectively provides two regioisomers, depending on the reaction pathway. An isocorrole species is the key intermediate to drive the reaction towards the 2-Br-17-nitro regioisomer.

Indexed as

Crystallography, X-RayHalogenationMolecular ConformationPorphyrinsSpectrophotometry, UltravioletStereoisomerism2-bromo-5-hydroxy-17-nitro-5,10,15-tris(4-methylphenyl)isocorrolecorrolePorphyrins

Identifiers

PMID21350743
PMCPMC3070944

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.