Evidence map›Paper›PMID 36053069›Full record

ArticleOrganic letters2022

Catalytic Access to 4-(sec-Alkyl)Anilines via 1,6-Conjugate Addition of Grignard Reagents to

Mercedes Zurro, Luo Ge, Syuzanna R Harutyunyan

Open access · hybridAbstract read
In one paragraph

Article in Organic letters, 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
0.8field-weighted citation impact, top 33% 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, 8 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

3 authors at 1 institution in 1 country.

Mercedes ZurroStratingh Institute for Chemistry University of Groningen Institution Nijenborgh 4, 9747 AG, Groningen, The Netherlands.
Luo GeStratingh Institute for Chemistry University of Groningen Institution Nijenborgh 4, 9747 AG, Groningen, The Netherlands.ORCID 0000-0001-9964-5156
Syuzanna R HarutyunyanStratingh Institute for Chemistry University of Groningen Institution Nijenborgh 4, 9747 AG, Groningen, The Netherlands.ORCID 0000-0003-2411-1250
University of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis of aniline derivatives, common building blocks in many pharmaceuticals, agrochemicals, dyes or polymers, has been limited to reactions based on benzene-toluene-xylene derivatives (BTX) due to their ample availability. Despite the large number of existing methodologies, the synthesis of chiral 4-(sec-alkyl)anilines has not been accomplished so far. In this work, a tandem strategy based on the generation of a reactive aza-

Indexed as

BenzeneXylenesAgrochemicalsAniline CompoundsCatalysisColoring AgentsIndicators and ReagentsIndolequinonesPharmaceutical PreparationsPolymersTolueneAgrochemicalsAniline CompoundsBenzeneColoring AgentsIndicators and ReagentsIndolequinonesPharmaceutical PreparationsPolymersquinone methideTolueneXylenes

Identifiers

PMID36053069
PMCPMC9486948
OpenAlexW4294281010

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.