Synthesis of Nitrogen Heterocycles Using Samarium(II) Iodide.

Open access · goldAbstract readReview

In one paragraph

Review in Molecules (Basel, Switzerland), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it

0cells of the map it votes in

2citing papers in PubMed

1.2field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 24 citations in OpenAlex.

Samarium(ii) iodide-mediated reactions applied to natural product total synthesis.RSC advances · 2022
Review
Selective C-N σ Bond Cleavage in Azetidinyl Amides under Transition Metal-Free Conditions.Molecules (Basel, Switzerland) · 2019
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

2 authors at 1 institution in 1 country.

Shicheng ShiDepartment of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, USA. ss2455@scarletmail.rutgers.edu.ORCID 0000-0001-8124-9235

Michal SzostakDepartment of Chemistry, Rutgers University, 73 Warren Street, Newark, NJ 07102, USA. michal.szostak@rutgers.edu.ORCID 0000-0002-9650-9690

Rutgers, The State University of New Jersey · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nitrogen heterocycles represent vital structural motifs in biologically-active natural products and pharmaceuticals. As a result, the development of new, convenient and more efficient processes to

Indexed as

Chemistry Techniques, SyntheticBiological ProductsCyclizationIodidesNitrogenPharmaceutical PreparationsSamariumBiological ProductsIodidesNitrogenPharmaceutical PreparationsSamariumaminoketyl radicalsnitrogennitrogen heterocyclesradical cyclizationsradicalsreductive couplingsamarium diiodidesamarium iodideSmI2umpolung cyclizations

Identifiers

PMID29160806

DOI10.3390/molecules22112018

PMCPMC6150357

OpenAlexW2771023871

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.