Evidence map›Paper›PMID 35492503›Full record

ArticleRSC advances2021

A library of new bifunctional alkenes obtained by a highly regiodivergent silylation of 1,5-hexadiene.

Rafał Januszewski, Bartosz Orwat, Jan Merna, Ireneusz Kownacki

Abstract read
In one paragraph

Article in RSC advances, 2021. 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.

Rafał JanuszewskiFaculty of Chemistry, Adam Mickiewicz University in Poznan Uniwersytetu Poznanskiego 8 61-614 Poznan Poland r.janusz@amu.edu.pl.ORCID https://orcid.org/0000-0002-5562-6647
Bartosz OrwatFaculty of Chemistry, Adam Mickiewicz University in Poznan Uniwersytetu Poznanskiego 8 61-614 Poznan Poland r.janusz@amu.edu.pl.ORCID https://orcid.org/0000-0003-1210-0095
Jan MernaUniversity of Chemistry and Technology in Prague Technická 5 166 28 Prague 6 Czech Republic.ORCID https://orcid.org/0000-0002-6508-0844
Ireneusz KownackiFaculty of Chemistry, Adam Mickiewicz University in Poznan Uniwersytetu Poznanskiego 8 61-614 Poznan Poland r.janusz@amu.edu.pl.ORCID https://orcid.org/0000-0002-5445-760X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An efficient methodology for the synthesis of two groups of silicon-containing alkenes is reported. It includes a highly regioselective functionalization of 1,5-hexadiene through hydrosilylation and dehydrogenative silylation with organofunctional silanes and siloxanes. The established conditions enable selective monofunctionalization of 1,5-hexadiene regardless of the organosilicon modifier used as well as the type of functional group bonded to the silicon-based compound. All products were isolated and fully characterized by NMR spectroscopy and MS techniques.

Identifiers

PMID35492503
PMCPMC9044431

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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.