Evidence map›Paper›PMID 30229798›Full record

ArticleOrganic & biomolecular chemistry2018

Stereo- and regioselective photocycloaddition of extended alkenes using γ-cyclodextrin.

Akshay Kashyap, Treyvon K Bokosike, Nattamai Bhuvanesh, Mahesh Pattabiraman

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Organic & biomolecular chemistry, 2018. 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
–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

1 citing paper in PubMed.

  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

4 authors.

Akshay KashyapDepartment of Chemistry, University of Nebraska Kearney, NE-68845, USA. pattabiramm2@unk.edu.
Treyvon K Bokosike
Nattamai Bhuvanesh
Mahesh Pattabiraman

Funding

Tracking and Evaluation CoreU54GM115458 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI GUDA, CHITTIBABU · 2016 to 2025
$42.8M
NIGMS NIH HHS U54 GM115458
6 · The paper itself

Abstract

Photoexcitation of dibenzalacetones (1a-d) in homogeneous media and solid state yields a mixture of products with poor conversions. Irradiation of the reactants complexed to γ-cyclodextrin predominantly affords a single dimer (syn adduct 6) despite the possibility for several monomeric and dimeric products. High selectivity in the cavitand-mediated reaction along with the structural characterization of the inclusion complex provides insight into the supramolecular interactions that drive the self-assembly of the host-guest system.

Indexed as

AlkenesBridged-Ring CompoundsChalconesCucurbit(n)urilsCycloaddition ReactionDimerizationgamma-CyclodextrinsImidazolesLightMacrocyclic CompoundsModels, MolecularStereoisomerismAlkenesBridged-Ring CompoundsChalconescucurbit(8)urilCucurbit(n)urilsgamma-cyclodextringamma-CyclodextrinsImidazolesMacrocyclic Compounds

Identifiers

PMID30229798
PMCPMC6215711

What OpenQuestion holds

Textmetadata
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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.