Evidence map›Paper›PMID 37110811›Full record

ArticleMolecules (Basel, Switzerland)2023

Synthesis and Properties of 1,3-Disubstituted Ureas Containing (Adamantan-1-yl)(phenyl)methyl Fragment Based on One-Pot Direct Adamantane Moiety Inclusion.

Vladimir D'yachenko, Dmitry Danilov, Yaroslav Kuznetsov, Semyon Moiseev, Vladimir Mokhov, Vladimir Burmistrov, Gennady Butov

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2023. 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
0.7field-weighted citation impact, top 30% 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, 4 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

7 authors at 1 institution in 1 country.

Vladimir D'yachenkoDepartment of Technology of Organic and Petrochemical Synthesis, Volgograd State Technical University (VSTU), 28 Lenin Avenue, Volgograd 400005, Russia.ORCID 0000-0002-6209-7106
Dmitry DanilovDepartment of Technology of Organic and Petrochemical Synthesis, Volgograd State Technical University (VSTU), 28 Lenin Avenue, Volgograd 400005, Russia.ORCID 0000-0001-8734-2617
Yaroslav KuznetsovDepartment of Technology of Organic and Petrochemical Synthesis, Volgograd State Technical University (VSTU), 28 Lenin Avenue, Volgograd 400005, Russia.ORCID 0000-0002-1933-2684
Semyon MoiseevVolzhsky Polytechnic Institute (Branch), Volgograd State Technical University (VSTU), 42a Engels Street, Volzhsky 404121, Russia.ORCID 0000-0003-0480-9096
Vladimir MokhovDepartment of Technology of Organic and Petrochemical Synthesis, Volgograd State Technical University (VSTU), 28 Lenin Avenue, Volgograd 400005, Russia.ORCID 0000-0003-2984-1877
Vladimir BurmistrovDepartment of Technology of Organic and Petrochemical Synthesis, Volgograd State Technical University (VSTU), 28 Lenin Avenue, Volgograd 400005, Russia.ORCID 0000-0002-8547-9166
Gennady ButovDepartment of Technology of Organic and Petrochemical Synthesis, Volgograd State Technical University (VSTU), 28 Lenin Avenue, Volgograd 400005, Russia.ORCID 0000-0002-0839-4513
Volgograd State Technical University · RU

Funding

Russian Science Foundation 19-73-10002
6 · The paper itself

Abstract

A one-stage method for the preparation of 1-[isocyanato(phenyl)methyl]adamantane containing a phenylmethylene fragment located between the adamantane fragment and the isocyanate group, and 1-[isocyanato(phenyl)methyl]-3,5-dimethyladamantane with additional methyl groups at the nodal positions of adamantane, with a yield of 95% and 89%, respectively, is described. The method includes the direct inclusion of an adamantane moiety through the reaction of phenylacetic acid ethyl ester with 1,3-dehydroadamantane or 3,5-dimethyl-1,3-dehydroadamantane followed by the hydrolysis of the obtained esters. The reaction of 1-[isocyanato(phenyl)methyl]adamantane with fluorine(chlorine)-containing anilines gave a series of 1,3-disubstituted ureas with 25-85% yield. 1-[Isocyanato(phenyl)methyl]-3,5-dimethyladamantane was involved in the reactions with fluorine(chlorine)-containing anilines and trans-4-amino-(cyclohexyloxy)benzoic acid to obtain another series of ureas with a yield of 29-74%. The resulting 1,3-disubstituted ureas are promising inhibitors of the human soluble epoxide hydrolase (hsEH).

Indexed as

1,3-disubstituted ureaadamantanehsEHisocyanatesoluble epoxide hydrolaseurea

Identifiers

PMID37110811
PMCPMC10143370
OpenAlexW4366595363

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.