Evidence map›Paper›PMID 38655462›Full record

ReviewRSC advances2024

Exploring the synthetic potential of epoxide ring opening reactions toward the synthesis of alkaloids and terpenoids: a review.

Madiha Hanif, Ameer Fawad Zahoor, Muhammad Jawwad Saif, Usman Nazeer, Kulsoom Ghulam Ali, Bushra Parveen, Asim Mansha, Aijaz Rasool Chaudhry, Ahmad Irfan

Abstract readReview
In one paragraph

Review in RSC advances, 2024. 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. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. 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

9 authors.

Madiha HanifDepartment of Chemistry, Government College University Faisalabad 38000-Faisalabad Pakistan fawad.zahoor@gcuf.edu.pk.
Ameer Fawad ZahoorDepartment of Chemistry, Government College University Faisalabad 38000-Faisalabad Pakistan fawad.zahoor@gcuf.edu.pk.ORCID https://orcid.org/0000-0003-2127-8848
Muhammad Jawwad SaifDepartment of Applied Chemistry, Government College University Faisalabad 38000-Faisalabad Pakistan.ORCID https://orcid.org/0000-0002-9589-876X
Usman NazeerDepartment of Chemistry, University of Houston 3585 Cullen Boulevard Texas 77204-5003 USA.
Kulsoom Ghulam AliDepartment of Chemistry, Government College University Faisalabad 38000-Faisalabad Pakistan fawad.zahoor@gcuf.edu.pk.
Bushra ParveenDepartment of Chemistry, Government College University Faisalabad 38000-Faisalabad Pakistan fawad.zahoor@gcuf.edu.pk.
Asim ManshaDepartment of Chemistry, Government College University Faisalabad 38000-Faisalabad Pakistan fawad.zahoor@gcuf.edu.pk.
Aijaz Rasool ChaudhryDepartment of Physics, College of Science, University of Bisha P.O. Box 551 Bisha 61922 Saudi Arabia.
Ahmad IrfanDepartment of Chemistry, King Khalid University P.O. Box 9004 Abha 61413 Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epoxides are oxygen containing heterocycles which are significantly employed as crucial intermediates in various organic transformations. They are considered highly reactive three-membered heterocycles due to ring strain and they undergo epoxide ring opening reactions with diverse range of nucleophiles. Epoxide ring-opening reactions have gained prominence as flexible and effective means to obtain various functionalized molecules. These reactions have garnered substantial attention in organic synthesis, driven by the need to comprehend the synthesis of biologically and structurally important organic compounds. They have also found applications in the synthesis of complex natural products. In this review article, we have summarized the implementation of epoxide ring opening reactions in the synthesis of alkaloids and terpenoids based natural products reported within the last decade (2014-2023).

Identifiers

PMID38655462
PMCPMC11036177

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.