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New mode of asymmetric induction for enantioselective radical N-heterobicyclization via kinetically stable chiral radical center

Chem(2023)10.1016/j.chempr.2023.09.010Source: DataRank Database

New mode of asymmetric induction for enantioselective radical N-heterobicyclization via kinetically stable chiral radical center is a research paper published in Chem (2023). On theSindex it has a DataRank of 0. It has been cited 30 times.

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0DataRank · unranked

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Open Access30 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)Impact (FWCI 3.41)OA: bronzeTopics (27)Linked Datasets (3)DataCite Reuse (3)IDs (PubMed, PMC, OpenAlex)

FAIR Checklist

Context only (not used in score)

Findable (2/2)

Has DOI
Indexed in repositories

Accessible (1/2)

Open Access

Interoperable (2/2)

DataCite relations
Linked datasets

Reusable (0/3)

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Authors (5)

Duo‐Sheng Wang ORCID,Zhenyu Zhu ORCID,Arghya Deb ORCID,X. Peter Zhang ORCID,Hao Xu ORCID

Live enrichment

PubMed:38313041 PMC:PMC10836202 OpenAlex:https://openalex.org/W4387540585

National Institutes of Health

Grant: R01-GM102554

National Science Foundation

Grant: CHE-2154885

National Science Foundation

Grant: S10-OD026910

National Science Foundation

Grant: CHE-2117246

NIGMS NIH HHS

Grant: R01 GM102554

NIH HHS

Grant: S10 OD026910

FWCI

3.41

Citation Percentile

0.9%

Citation Trend

2024

2025

2026

bronzeLicense: http://www.elsevier.com/open-access/userlicense/1.0/

journalhttp://www.cell.com/article/S2451929423004655/pdf

publisherhttp://www.cell.com/article/S2451929423004655/pdf

publisherhttps://api.elsevier.com/content/article/PII:S2451929423004655?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2451929423004655?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.chempr.2023.09.010

Fields of Study

Synthesis and Catalytic ReactionsCatalytic C–H Functionalization MethodsRadical Photochemical Reactions

Keywords

Enantioselective synthesisChemistrySteric effectsStereospecificityAsymmetric inductionLigand (biochemistry)StereoselectivityCombinatorial chemistryCatalysisReactivity (psychology)Radical cyclizationChiral ligandStereochemistryBicyclic moleculeOrganic chemistryReceptorRadical ReactionMetalloradical Catalysis5-Exo-trig6-Endo-trig[3.1.0]-Bicyclic AziridinesAllyl Sulfamoyl AzidesHeterobicyclizationStable Chiral Radical

CCDC 2211360: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc2d736zCambridge Crystallographic Data Centre

CCDC 2211361: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc2d7370Cambridge Crystallographic Data Centre

CCDC 2106738: Experimental Crystal Structure Determination

10.5517/ccdc.csd.cc28q79kCambridge Crystallographic Data Centre