Evidence map›Paper›PMID 30112083›Full record

ReviewBeilstein journal of organic chemistry2018

Synthesis of spirocyclic scaffolds using hypervalent iodine reagents.

Fateh V Singh, Priyanka B Kole, Saeesh R Mangaonkar, Samata E Shetgaonkar

Open access · diamondAbstract readReview
In one paragraph

Review in Beilstein journal of organic chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Hypervalent iodine-mediated intramolecular alkene halocyclisation.Beilstein journal of organic chemistry · 2024
    Review
  3. Review
  4. Article
  5. Iodine(V)-Based Oxidants in Oxidation Reactions.Molecules (Basel, Switzerland) · 2023
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. 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

4 authors at 1 institution in 1 country.

Fateh V SinghChemistry Division, School of Advanced Sciences (SAS), VIT University, Chennai Campus, Chennai-600 127, Tamil Nadu, India.
Priyanka B KoleChemistry Division, School of Advanced Sciences (SAS), VIT University, Chennai Campus, Chennai-600 127, Tamil Nadu, India.
Saeesh R MangaonkarChemistry Division, School of Advanced Sciences (SAS), VIT University, Chennai Campus, Chennai-600 127, Tamil Nadu, India.
Samata E ShetgaonkarChemistry Division, School of Advanced Sciences (SAS), VIT University, Chennai Campus, Chennai-600 127, Tamil Nadu, India.
Vellore Institute of Technology University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypervalent iodine reagents have been developed as highly valuable reagents in synthetic organic chemistry during the past few decades. These reagents have been identified as key replacements of various toxic heavy metals in organic synthesis. Various synthetically and biologically important scaffolds have been developed using hypervalent iodine reagents either in stoichiometric or catalytic amounts. In addition, hypervalent iodine reagents have been employed for the synthesis of spirocyclic scaffolds via dearomatization processes. In this review, various approaches for the synthesis of spirocyclic scaffolds using hypervalent iodine reagents are covered including their stereoselective synthesis. Additionally, the applications of these reagents in natural product synthesis are also covered.

Indexed as

hypervalent iodine reagentsiodoarenesnatural productsoxidative cyclizationspirocyclic compounds

Identifiers

PMID30112083
PMCPMC6071689
OpenAlexW2883673573

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.