Evidence map›Paper›PMID 37649665›Full record

ArticleRSC advances2023

Diastereospecific arylation and cascade deconstructive amidation/thioesterification of readily available lactam-fused bromolactones.

Minh Do, Stella I Anosike, Timothy K Beng

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

3 authors at 1 institution in 1 country.

Minh DoDepartment of Chemistry, Central Washington University Ellensburg WA 98926 USA Timothy.beng@cwu.edu.
Stella I AnosikeDepartment of Chemistry, Central Washington University Ellensburg WA 98926 USA Timothy.beng@cwu.edu.
Timothy K BengDepartment of Chemistry, Central Washington University Ellensburg WA 98926 USA Timothy.beng@cwu.edu.ORCID https://orcid.org/0000-0002-4364-5664
Central Washington University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An intrinsic goal when designing synthetic methodology is to identify approaches whereby readily accessible precursors are converted into an array of products, which efficiently tap into new 3D-chemical space. In these studies, readily available bicyclic lactam-bromolactones have been interrogated in several fragment growth protocols by utilizing the halogen and lactone motifs as versatile linchpins for strategic construction of C-C, C-N, C-O, and C-S bonds. Diastereospecific C(sp

Identifiers

PMID37649665
PMCPMC10463012
OpenAlexW4386267701

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.