Evidence map›Paper›PMID 33721275›Full record

ArticlePhotochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology2021

Light-triggered elimination of CO

Qianghua Lin, Manabu Abe

Abstract read
PubMed Publisher
In one paragraph

Article in Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Qianghua LinDepartment of Chemistry, Graduate School of Science, Hiroshima University, Higashihiroshima, Hiroshima, 739-8526, Japan.
Manabu AbeDepartment of Chemistry, Graduate School of Science, Hiroshima University, Higashihiroshima, Hiroshima, 739-8526, Japan. mabe@hiroshima-u.ac.jp.ORCID http://orcid.org/0000-0002-2013-4394

Funding

Japan Society for the Promotion of Science 17H03022Japan Society for the Promotion of Science 20K21197
6 · The paper itself

Abstract

A new chromophore, 2-(4-nitrophenyl)-1H-indole (NPI), was synthesized as a potential photolabile protecting group. Caged benzoic acids featuring the NPI chromophore were synthesized as model compounds. Benzoic acid was released in moderate yields (~ 40-60%) upon photolysis of the caged benzoic acids without any additional chemical reagents. Interestingly, an aldehyde, 1-(5-(1-formyl-1H-indol-2-yl)-2-nitrophenyl)ethyl benzoate, was isolated in ≈ 20% together with benzoic acid (≈ 40%) in photolysis of a caged benzoic acid, 2-(2-(3-(1-(benzoyloxy)ethyl)-4-nitrophenyl)-1H-indol-1-yl)acetic acid. The functional group, CH

Indexed as

Electron transferIndolesLaser flash photolysisPhotochemical decarboxylation

Identifiers

PMID33721275

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.