Evidence map›Paper›PMID 34667540›Full record

ArticleChemical science2021

Oxa-spirocycles: synthesis, properties and applications.

Kateryna Fominova, Taras Diachuk, Dmitry Granat, Taras Savchuk, Vladyslav Vilchynskyi, Oleksiy Svitlychnyi, Vladyslav Meliantsev, Igor Kovalchuk, Eduard Litskan, Vadym V Levterov and 17 more

Abstract read
In one paragraph

Article in Chemical science, 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. Article
  2. Synthesis ofThe Journal of organic chemistry · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. C-H Insertion via Ruthenium CatalyzedJournal of the American Chemical Society · 2022
    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

27 authors.

Kateryna FominovaEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Taras DiachukEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Dmitry GranatEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Taras SavchukEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Vladyslav VilchynskyiEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.ORCID https://orcid.org/0000-0002-5074-4433
Oleksiy SvitlychnyiEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Vladyslav MeliantsevEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Igor KovalchukEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Eduard LitskanEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Vadym V LevterovEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Valentyn R BadloEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Ruslan I VaskevychInstitute of Organic Chemistry, National Academy of Sciences of Ukraine Murmanska St. 5 02094 Kyiv Ukraine.
Alla I VaskevychNational Technical University of Ukraine, Igor Sikorsky Kiev Polytechnic Institute Prosp. Peremohy 37 03056 Kyiv Ukraine.
Andrii V BolbutInstitute of Organic Chemistry, National Academy of Sciences of Ukraine Murmanska St. 5 02094 Kyiv Ukraine.
Volodymyr V SemenoEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.ORCID https://orcid.org/0000-0001-6609-8301
Rustam IminovEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Kostiantyn ShvydenkoInstitute of Organic Chemistry, National Academy of Sciences of Ukraine Murmanska St. 5 02094 Kyiv Ukraine.
Anastasiia S KuznetsovaNational Research Tomsk Polytechnic University Lenin Ave. 30 634050 Tomsk Russia.
Yurii V DmytrivEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Daniil VysochynEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Vasyl RipenkoEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Andrei A TolmachevEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.
Olexandra PavlovaBienta Chervonotkatska 78 02094 Kyiv Ukraine http://www.bienta.net.
Halyna KuznietsovaBienta Chervonotkatska 78 02094 Kyiv Ukraine http://www.bienta.net.ORCID https://orcid.org/0000-0002-1296-1007
Iryna PishelBienta Chervonotkatska 78 02094 Kyiv Ukraine http://www.bienta.net.ORCID https://orcid.org/0000-0002-5267-6817
Petro BoryskoBienta Chervonotkatska 78 02094 Kyiv Ukraine http://www.bienta.net.ORCID https://orcid.org/0000-0002-5840-5233
Pavel K MykhailiukEnamine Ltd Chervonotkatska 78 02094 Kyiv Ukraine Pavel.Mykhailiuk@gmail.com http://www.enamine.net http://www.mykhailiukchem.org.ORCID https://orcid.org/0000-0003-1821-9011

Funding

European Research Council 101000893
6 · The paper itself

Abstract

A general approach to a new generation of spirocyclic molecules - oxa-spirocycles - was developed. The key synthetic step was iodocyclization. More than 150 oxa-spirocyclic compounds were prepared. Incorporation of an oxygen atom into the spirocyclic unit dramatically improved water solubility (by up to 40 times) and lowered lipophilicity. More potent oxa-spirocyclic analogues of antihypertensive drug terazosin were synthesized and studied

Identifiers

PMID34667540
PMCPMC8447932

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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.