Evidence map›Paper›PMID 35938223›Full record

ArticleOrganic & biomolecular chemistry2022

Combining iminium and supramolecular catalysis for the [4 + 2] cycloaddition of

Kendra K Shrestha, Michael A Hilyard, Indunil Alahakoon, Michael C Young

Abstract read
In one paragraph

Article in Organic & biomolecular chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Kendra K ShresthaDepartment of Chemistry & Biochemistry, School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft St., Mailstop 602, Toledo, OH 43606, USA. michael.young8@utoledo.edu.
Michael A HilyardDepartment of Chemistry & Biochemistry, School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft St., Mailstop 602, Toledo, OH 43606, USA. michael.young8@utoledo.edu.ORCID 0000-0002-5710-0403
Indunil AlahakoonDepartment of Chemistry & Biochemistry, School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft St., Mailstop 602, Toledo, OH 43606, USA. michael.young8@utoledo.edu.
Michael C YoungDepartment of Chemistry & Biochemistry, School of Green Chemistry and Engineering, The University of Toledo, 2801 W. Bancroft St., Mailstop 602, Toledo, OH 43606, USA. michael.young8@utoledo.edu.ORCID 0000-0002-3256-5562

Funding

Late Stage Derivitization of Complex Molecules via Hydrogen Bond-Directed C-H FunctionalizationR15GM131362 · NIGMS · UNIVERSITY OF TOLEDO · PI YOUNG, MICHAEL C · 2019 to 2019
$451k
NIGMS NIH HHS R15 GM131362
6 · The paper itself

Abstract

Herein we describe a method for combining supramolecular catalysis with imininum-based organocatalysis in the Diels-Alder cycloaddition reaction. Both supramolecular host and L-proline are required for the reaction to occur, implying that encapsulation of the substrates and co-catalyst are necessary for the reaction to occur. We explore the substrate scope for a variety of

Indexed as

Cycloaddition ReactionAcroleinCatalysisMolecular StructureStereoisomerismAcroleincinnamaldehyde

Identifiers

PMID35938223
PMCPMC9462845

What OpenQuestion holds

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Registered trials

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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.