Evidence map›Paper›PMID 36558094›Full record

ArticleMolecules (Basel, Switzerland)2022

A Green Blue LED-Driven Two-Liquid-Phase One-Pot Procedure for the Synthesis of Estrogen-Related Quinol Prodrugs.

Elisa De Marchi, Lorenzo Botta, Bruno Mattia Bizzarri, Raffaele Saladino

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. 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
0.2field-weighted citation impact, top 52% of its field
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, 2 citations in OpenAlex.

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

4 authors at 1 institution in 1 country.

Elisa De MarchiDepartment of Biological and Ecological Sciences, University of Tuscia, 01100 Viterbo, Italy.ORCID 0000-0001-6116-9772
Lorenzo BottaDepartment of Biological and Ecological Sciences, University of Tuscia, 01100 Viterbo, Italy.ORCID 0000-0002-0856-2986
Bruno Mattia BizzarriDepartment of Biological and Ecological Sciences, University of Tuscia, 01100 Viterbo, Italy.ORCID 0000-0001-7085-5432
Raffaele SaladinoDepartment of Biological and Ecological Sciences, University of Tuscia, 01100 Viterbo, Italy.ORCID 0000-0002-4420-9063
Università degli Studi della Tuscia · IT

Funding

Ministry of Education, Universities and Research cod. 2017BMK8JR
6 · The paper itself

Abstract

Quinol derivatives of estrogens are effective pro-drugs in steroid replacement therapy. Here, we report that these compounds can be synthesized in one-pot conditions and high yield by blue LED-driven photo-oxygenation of parent estrogens. The oxidation was performed in buffer and eco-certified 2-methyltetrahydrofuran as the two-liquid-phase reaction solvent, and in the presence of meso-tetraphenyl porphyrin as the photosensitizer. Two steroidal prodrugs 10β, 17β-dihydroxyestra-1,4-dien-3-one (DHED) and 10β-Hydroxyestra-1,4-diene-3,17-dione (HEDD) were obtained with high yield and selectivity.

Indexed as

EstradiolProdrugsEstrogensHydroquinonesEstradiolEstrogenshydroquinoneHydroquinonesProdrugsCNS-selective estrogen therapyDHEDestrogen-related quinolsestrogensHEDDneuroprotectionpara-quinolphotochemistryphoto-oxygenationprodrug

Identifiers

PMID36558094
PMCPMC9782465
OpenAlexW4312195700

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.