Evidence map›Paper›PMID 34847327›Full record

ArticleAccounts of chemical research2021

A New Paradigm in Enantioselective Cobalt Catalysis: Cationic Cobalt(I) Catalysts for Heterodimerization, Cycloaddition, and Hydrofunctionalization Reactions of Olefins.

Souvagya Biswas, Mahesh M Parsutkar, Stanley M Jing, Vinayak V Pagar, James H Herbort, T V RajanBabu

Open access · greenAbstract read
In one paragraph

Article in Accounts of chemical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.6field-weighted citation impact, top 4% of its field
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

23 citing papers in PubMed, 85 citations in OpenAlex.

  1. Cobalt-Catalyzed Migratory E-Selective Asymmetric Aza-Nozaki-Hiyama-Kishi Coupling.Angewandte Chemie (International ed. in English) · 2026
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  15. Asymmetric formal spNature communications · 2023
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  16. JACS Au · 2023
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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

6 authors at 1 institution in 1 country.

Souvagya BiswasDepartment of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, United States.
Mahesh M ParsutkarDepartment of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0001-6320-2345
Stanley M JingDepartment of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0001-8952-4553
Vinayak V PagarDepartment of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0002-6729-693X
James H HerbortDepartment of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, United States.
T V RajanBabuDepartment of Chemistry and Biochemistry, The Ohio State University, 100 West 18th Avenue, Columbus, Ohio 43210, United States.ORCID 0000-0001-8515-3740
The Ohio State University · US

Funding

Highly Selective Catalytic Reactions of Alkenes and Alkynes Relevant to Medicinal and Process ChemistryR35GM139545 · NIGMS · OHIO STATE UNIVERSITY · PI RAJANBABU, T V · 2021 to 2025
$2.1M
New Alkene Chemistry for the Synthesis of Medicinally Relevant CompoundsR01GM108762 · NIGMS · OHIO STATE UNIVERSITY · PI RAJANBABU, T V · 2015 to 2018
$1.3M
NIGMS NIH HHS R01 GM108762NIGMS NIH HHS R35 GM139545
6 · The paper itself

Abstract

One of the major challenges facing organic synthesis in the 21st century is the utilization of abundantly available feedstock chemicals for fine chemical synthesis. Regio- and enantioselective union of easily accessible 1,3-dienes and other feedstocks like ethylene, alkyl acrylates, and aldehydes can provide valuable building blocks adorned with latent functionalities for further synthetic elaboration. Through an approach that relies on mechanistic insights and systematic examination of ligand and counterion effects, we developed an efficient cobalt-based catalytic system [(

Indexed as

AlkenesCobaltCatalysisCycloaddition ReactionMolecular StructureStereoisomerismAlkenesCobalt

Identifiers

PMID34847327
PMCPMC8721816
OpenAlexW3215994886

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.