Evidence map›Paper›PMID 31666880›Full record

ArticleBeilstein journal of organic chemistry2019

Indium-mediated C-allylation of melibiose.

Christian Denner, Manuel Gintner, Hanspeter Kählig, Walther Schmid

Open access · diamondAbstract read
In one paragraph

Article in Beilstein journal of organic chemistry, 2019. 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
0.2field-weighted citation impact, top 51% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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 at 1 institution in 1 country.

Christian DennerInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, A-1090, Vienna, Austria.ORCID https://orcid.org/0000-0001-5100-5854
Manuel GintnerInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, A-1090, Vienna, Austria.ORCID https://orcid.org/0000-0001-8503-3335
Hanspeter KähligInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, A-1090, Vienna, Austria.ORCID https://orcid.org/0000-0002-3898-6501
Walther SchmidInstitute of Organic Chemistry, University of Vienna, Währinger Straße 38, A-1090, Vienna, Austria.
University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The indium-mediated allylation reaction has been applied to melibiose, a disaccharidic substrate. This elongation methodology allows for a short, efficient and diastereoselective approach towards complex glycosylated carbohydrate structures. The stereochemical outcome of the key intermediates, allylated disaccharides, has been determined by X-ray analysis. Ozonolysis of the introduced double bond yielded the unprotected elongated disaccharides in the equilibrium of the pyranoid as well as furanoid isomers in both anomeric forms, respectively. Per-

Indexed as

carbohydratesC–C bond formationindium-mediated allylationmelibioseozonolysis

Identifiers

PMID31666880
PMCPMC6808214
OpenAlexW2981035614

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.