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A general N-alkylation platform via copper metallaphotoredox and silyl radical activation of alkyl halides

Chem(2021)10.1016/j.chempr.2021.05.005Source: DataRank Database

A general N-alkylation platform via copper metallaphotoredox and silyl radical activation of alkyl halides is a research paper published in Chem (2021). On theSindex it has a DataRank of 0. It has been cited 104 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access104 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (12 grants)Impact (FWCI 7.04)OA: bronzeTopics (27)IDs (PubMed, PMC, OpenAlex)SDGs (2)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (3)

Albert Cabré ORCID,David W. C. MacMillan ORCID,Nathan W. Dow ORCID

Live enrichment

PubMed:34423174 PMC:PMC8372964 OpenAlex:https://openalex.org/W3167687104

National Institute of General Medical Sciences

Grant: R35GM134897-01

NIGMS NIH HHS

Grant: R35 GM134897

National Institutes of Health

Grant: 1R35GM134897-01

Photoredox Catalysis Applications in Organometallics and Chemical Biology

Celgene

Bristol-Myers Squibb Co

Pfizer Ltd

Janssen LP

Merck & Co Inc

National Institutes of Health

Pfizer

Genentech

Princeton University

FWCI

7.04

Citation Percentile

1.0%

Citation Trend

2021

2022

2023

2024

2025

2026

bronzeLicense: Elsevier Non-Commercial

journalhttp://www.cell.com/article/S2451929421002540/pdf

publisherhttp://www.cell.com/article/S2451929421002540/pdf

publisherhttps://api.elsevier.com/content/article/PII:S2451929421002540?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S2451929421002540?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.chempr.2021.05.005

Fields of Study

Radical Photochemical ReactionsCatalytic C–H Functionalization MethodsSulfur-Based Synthesis Techniques01 natural sciences0104 chemical sciences

Keywords

NucleophileAlkylAlkylationChemistrySN2 reactionReactivity (psychology)HalideSteric effectsCatalysisCombinatorial chemistrySilylationRegioselectivityNucleophilic substitutionHalogenMedicinal chemistryOrganic chemistryN-alkylationCopper CatalysisPhotoredoxHalogen AbstractionCyclopropylationOrganochloride Activation

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Clean water and sanitation