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

Enantioselective regiospecific addition of propargyltrichlorosilane to aldehydes catalyzed by biisoquinoline N , N’ -dioxide

Beilstein Journal of Organic Chemistry(2024)10.3762/bjoc.20.255Source: DataRank Database

Enantioselective regiospecific addition of propargyltrichlorosilane to aldehydes catalyzed by biisoquinoline N , N’ -dioxide is a research paper published in Beilstein Journal of Organic Chemistry (2024). On theSindex it has a DataRank of 0. It has been cited 1 time.

N/A

0DataRank · unranked

Scored on demand from live citation data

Open Access1 citations

Download PDF

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 (4 grants)Impact (FWCI 0.20)OA: goldTopics (22)IDs (PubMed, PMC, OpenAlex)SDGs (1)

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 (7)

Sreerag N. Moorkkannur ORCID,Anne Burns,Layla Auter,Valentino Cesiliano ORCID,Rajeev Prabhakar ORCID

Live enrichment

PubMed:39624656 PMC:PMC11610484 OpenAlex:https://openalex.org/W4404703417

National Institutes of Health

Grant: 1R15GM139087-01

Enantioselective Catalytic Chlorosilane Reactions

National Science Foundation

Grant: CHE-2102563

NIGMS NIH HHS

Grant: R15 GM139087

National Science Foundation

Grant: 2102563

CAS: Development of Bio-inspired Catalysts for Hydrolysis: Insights from Theoretical Studies

FWCI

0.20

Citation Percentile

0.5%

Citation Trend

2025

goldLicense: cc-by

journalhttps://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-20-255.pdf

GOLDhttps://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-20-255.pdf

publisherhttps://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-20-255.pdf

publisherhttps://www.beilstein-journals.org/bjoc/articles/20/255

journalhttps://doi.org/10.3762/bjoc.20.255

Fields of Study

Asymmetric Synthesis and CatalysisOxidative Organic Chemistry ReactionsSynthetic Organic Chemistry MethodsMedicineChemistry01 natural sciences0104 chemical sciences

Keywords

Enantioselective synthesisChemistryCatalysisOrganic chemistryCombinatorial chemistryMedicinal chemistryOrganocatalysisComputational ChemistryLewis Base CatalysisPropargyltrichlorosilaneΑ-Allenic AlcoholQD241-441LetterScienceQ

Sustainable Development Goals

SDG 0: Clean water and sanitation