Evidence map›Paper›PMID 30117646›Full record

ArticleAngewandte Chemie (International ed. in English)2018

Synthesis of Spirocyclic Ethers by Enantioselective Copper-Catalyzed Carboetherification of Alkenols.

Shuklendu D Karyakarte, Chanchamnan Um, Ilyas A Berhane, Sherry R Chemler

Open access · greenAbstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 35 citations in OpenAlex.

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  10. Diastereoselective spACS catalysis · 2020
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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

4 authors at 1 institution in 1 country.

Shuklendu D KaryakarteDepartment of Chemistry, State University of New York at Buffalo, 618 Natural Science Complex, Buffalo, NY, 14260, USA.
Chanchamnan UmDepartment of Chemistry, State University of New York at Buffalo, 618 Natural Science Complex, Buffalo, NY, 14260, USA.
Ilyas A BerhaneDepartment of Chemistry, State University of New York at Buffalo, 618 Natural Science Complex, Buffalo, NY, 14260, USA.
Sherry R ChemlerDepartment of Chemistry, State University of New York at Buffalo, 618 Natural Science Complex, Buffalo, NY, 14260, USA.ORCID 0000-0001-6702-5032
University at Buffalo, State University of New York · US

Funding

New Methods for Nitrogen Heterocycle SynthesisR01GM078383 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI CHEMLER, SHERRY R · 2006 to 2023
$5.6M
NIGMS NIH HHS 078383NIGMS NIH HHS R01 GM078383
6 · The paper itself

Abstract

Spirocyclic ethers can be found in bioactive compounds. This copper-catalyzed enantioselective alkene carboetherification provides 5,5-, 5,6- and 6,6-spirocyclic products containing fully substituted chiral carbon centers with up to 99 % enantiomeric excess. This reaction features the formation of two rings from acyclic substrates, 1,1-disubstituted alkenols functionalized with either arenes, alkenes, or alkynes, and clearly constitutes a powerful way to synthesize chiral spirocyclic ethers.

Indexed as

AlkenesAlkynesCatalysisCopperCrystallography, X-RayEthersMolecular ConformationPropanolsSpiro CompoundsStereoisomerismAlkenesAlkynesallyl alcoholCopperEthersPropanolsSpiro Compoundscoppercyclizationsenantioselectivityspiro-compoundssynthetic methods

Identifiers

PMID30117646
PMCPMC6375082
OpenAlexW2885260618

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.