Evidence map›Paper›PMID 33926128›Full record

ReviewMolecules (Basel, Switzerland)2021

Diazocarbonyl and Related Compounds in the Synthesis of Azoles.

Anton Budeev, Grigory Kantin, Dmitry Dar'in, Mikhail Krasavin

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2021. 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. Cascade transformation of 2-(diazoacetyl)-2Beilstein journal of organic chemistry · 2026
    Article
  3. Article
  4. PROTACs in the Management of Prostate Cancer.Molecules (Basel, Switzerland) · 2023
    Review
  5. Article
  6. New Antifungal Agents with Azole Moieties.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  7. Review
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.

Anton BudeevInstitute of Chemistry, St. Petersburg State University, 198504 Peterhof, Russia.
Grigory KantinInstitute of Chemistry, St. Petersburg State University, 198504 Peterhof, Russia.
Dmitry Dar'inInstitute of Chemistry, St. Petersburg State University, 198504 Peterhof, Russia.ORCID 0000-0002-0413-7413
Mikhail KrasavinInstitute of Chemistry, St. Petersburg State University, 198504 Peterhof, Russia.ORCID 0000-0002-0200-4772

Funding

Russian Science Support Foundation 20-13-00024
6 · The paper itself

Abstract

Diazocarbonyl compounds have found numerous applications in many areas of chemistry. Among the most developed fields of diazo chemistry is the preparation of azoles from diazo compounds. This approach represents a useful alternative to more conventional methods of the synthesis of azoles. A comprehensive review on the preparation of various azoles (oxazoles, thiazoles, imidazoles, pyrazoles, triazoles, and tetrazoles) from diazocarbonyl and related compounds is presented for the first time along with discussion of advantages and disadvantages of «diazo» approaches to azoles.

Indexed as

atom economyazolesdiazocarbonyl compounds

Identifiers

PMID33926128
PMCPMC8123665

What OpenQuestion holds

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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.