Evidence map›Paper›PMID 40190640›Full record

ArticleRSC advances2025

Sequential Michael addition, cross-coupling and [3 + 2] cycloaddition reactions within the coordination sphere of chiral Ni(ii) Schiff base complexes derived from dehydroamino acids: pathways to the asymmetric synthesis of structurally diverse

Emma A Khachatryan, Lusine Yu Sahakyan, Anna S Tovmasyan, Gagik S Melikyan, Henrik A Panosyan, Anna F Mkrtchyan, Norio Shibata, Andrei V Malkov, Ashot S Saghyan

Abstract read
In one paragraph

Article in RSC advances, 2025. 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

9 authors.

Emma A KhachatryanInstitute of Pharmacy, Yerevan State University 1 Alex Manoogian Str. 0025 Yerevan Armenia anna_mkrtchyan@ysu.am +374 60 710 410 +374 60 710 427.
Lusine Yu SahakyanInstitute of Pharmacy, Yerevan State University 1 Alex Manoogian Str. 0025 Yerevan Armenia anna_mkrtchyan@ysu.am +374 60 710 410 +374 60 710 427.
Anna S TovmasyanScientific and Production Center "Armbiotechnology" of NAS RA 14 Gyurjyan Str. 0056 Yerevan Armenia.
Gagik S MelikyanInstitute of Pharmacy, Yerevan State University 1 Alex Manoogian Str. 0025 Yerevan Armenia anna_mkrtchyan@ysu.am +374 60 710 410 +374 60 710 427.
Henrik A PanosyanScientific and Technological Center of Organic and Pharmaceutical Chemistry of NAS RA 26 Azatutyan Ave. 0014 Yerevan Armenia.
Anna F MkrtchyanInstitute of Pharmacy, Yerevan State University 1 Alex Manoogian Str. 0025 Yerevan Armenia anna_mkrtchyan@ysu.am +374 60 710 410 +374 60 710 427.ORCID https://orcid.org/0000-0003-0325-1799
Norio ShibataDepartment of Life Science and Applied Chemistry, Nagoya Institute of Technology Showa-ku Nagoya 466-8555 Japan.ORCID https://orcid.org/0000-0002-3742-4064
Andrei V MalkovDepartment of Chemistry, Loughborough University, University Road Loughborough LE11 3TU UK.ORCID https://orcid.org/0000-0001-6072-2353
Ashot S SaghyanInstitute of Pharmacy, Yerevan State University 1 Alex Manoogian Str. 0025 Yerevan Armenia anna_mkrtchyan@ysu.am +374 60 710 410 +374 60 710 427.ORCID https://orcid.org/0000-0002-3124-170X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An approach to the synthesis of a series of novel, enantiomerically pure analogs of β-hydroxy-α-amino acids is reported. The method involves the introduction of the acetylene group into their side chain, followed by further elaboration of the terminal alkyne moiety. The asymmetric synthesis of alkyl- and aryl-substituted derivatives of (

Identifiers

PMID40190640
PMCPMC11969660

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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.