Evidence map›Paper›PMID 30517785›Full record

ArticleJournal of the American Chemical Society2018

Nickel-Catalyzed Reductive [2+2] Cycloaddition of Alkynes.

Santiago Cañellas, John Montgomery, Miquel À Pericàs

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2018. 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.

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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.

Santiago CañellasInstitute of Chemical Research of Catalonia (ICIQ), The Barcelona Institute of Science and Technology , Avda. Països Catalans 16 , E-43007 Tarragona , Spain.ORCID 0000-0002-8700-4615
John MontgomeryDepartment of Chemistry , University of Michigan , 930 North University Avenue , Ann Arbor , Michigan 48019-1055 , United States.ORCID 0000-0002-2229-0585
Miquel À PericàsInstitute of Chemical Research of Catalonia (ICIQ), The Barcelona Institute of Science and Technology , Avda. Països Catalans 16 , E-43007 Tarragona , Spain.ORCID 0000-0003-0195-8846

Funding

Supplement: Regio- and Site-Selective Processes Using Transition Metal and Biological CatalystsR35GM118133 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JOHN MONTGOMERY · 2016 to 2026
$4.9M
NIGMS NIH HHS R35 GM118133
6 · The paper itself

Abstract

The nickel-catalyzed synthesis of tetrasubstituted cyclobutenes from alkynes is reported. This transformation is uniquely promoted by the use of a primary aminophosphine, an unusual ligand in nickel catalysis. Mechanistic insights for this new transformation are provided, and postreaction modifications of the cyclobutene products to stereodefined cyclic and acyclic compounds are reported, including the synthesis of epi-truxillic acid.

Indexed as

AlkynesCatalysisCycloaddition ReactionCyclobutanesLigandsModels, ChemicalNickelOxidation-ReductionPhosphinesAlkynesCyclobutanesLigandsNickelPhosphines

Identifiers

PMID30517785
PMCPMC6470007

What OpenQuestion holds

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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.