Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

A Green, Facile Method for Selective α-Bromination of Flavanones

ACS Omega(2025)10.1021/acsomega.5c07396Source: DataRank Database

A Green, Facile Method for Selective α-Bromination of Flavanones is a research paper published in ACS Omega (2025). On theSindex it has a DataRank of 0.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access0 citations

Free full text

Cite:

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (2 grants)Impact (FWCI 0.00)OA: goldTopics (12)IDs (PubMed, OpenAlex)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

Authors (9)

Tatiana N. Laremore ORCID,Hemant P. Yennawar ORCID,Gena D. Guerin,Brendan Pelletier,Samreen Dallal

Live enrichment

PubMed:41487166 OpenAlex:https://openalex.org/W4417433268

National Institutes of Health

Grant: 1S10OD02858901

National Institutes of Health

Grant: 1S10RR02343901

FWCI

0.00

Citation Percentile

0.2%

goldLicense: cc-by-nc-nd

journalhttps://pubs.acs.org/doi/pdf/10.1021/acsomega.5c07396?ref=article_openPDF

publisherhttps://pubs.acs.org/doi/pdf/10.1021/acsomega.5c07396?ref=article_openPDF

publisherhttps://pubs.acs.org/doi/pdf/10.1021/acsomega.5c07396

journalhttps://doi.org/10.1021/acsomega.5c07396

repositoryhttps://pubmed.ncbi.nlm.nih.gov/41487166

Fields of Study

Vanadium and Halogenation ChemistryOxidative Organic Chemistry ReactionsBioactive natural compounds

Keywords

HalogenationFlavanoneElectrospray ionizationFlavonoidPolyphenolSelectivityLead compoundBromideMass spectrometry