Evidence map›Paper›PMID 33629454›Full record

ReviewAngewandte Chemie (International ed. in English)2021

Recent Advances in Photoredox-Mediated Radical Conjugate Addition Reactions: An Expanding Toolkit for the Giese Reaction.

Anastasia L Gant Kanegusuku, Jennifer L Roizen

Abstract readReview
In one paragraph

Review in Angewandte Chemie (International ed. in English), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
–field-weighted citation impact
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

60 citing papers in PubMed.

  1. Article
  2. Acridine/Lewis acid photocatalysis enables α-amidyl radical cyclizations.Organic chemistry frontiers : an international journal of organic chemistry · 2026
    Article
  3. Article
  4. Photoredox-Catalyzed Lysine C(spJournal of the American Chemical Society · 2026
    Article
  5. Article
  6. Densely-functionalized bicyclic cyclopentanones by combined photoinduced 6-Organic chemistry frontiers : an international journal of organic chemistry · 2026
    Article
  7. Pyridine-boryl radical mediated synthesis of quinolinesOrganic chemistry frontiers : an international journal of organic chemistry · 2026
    Article
  8. Nickel-Catalyzed Twofold Conjunctive Coupling via Philicity-Alternating Radical Relay.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  9. Boron-Mediated Hydroalkylation of Unactivated Olefins: AnJournal of the American Chemical Society · 2026
    Article
  10. Article
  11. Article
  12. Bimolecular Homolytic Substitution (SACS central science · 2025
    Review
  13. Methyl Radical Addition Reactions to C═X Double Bonds.The Journal of organic chemistry · 2025
    Article
  14. Article
  15. Photocatalytic Generation of a Ground-State Electron Donor Through Water Activation.Angewandte Chemie (International ed. in English) · 2025
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Iterative One-Carbon Homologation of Unmodified Carboxylic Acids.Journal of the American Chemical Society · 2024
    Article
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

2 authors.

Anastasia L Gant KanegusukuDepartment of Chemistry, Duke University, Box 90346, Durham, NC, 27708-0354, USA.ORCID 0000-0001-9961-6398
Jennifer L RoizenDepartment of Chemistry, Duke University, Box 90346, Durham, NC, 27708-0354, USA.ORCID 0000-0002-6053-5512

Funding

Exploiting Masked Alcohols to Guide Atom-Transfer ReactionsR35GM128741 · NIGMS · DUKE UNIVERSITY · PI ROIZEN, JENNIFER L · 2018 to 2020
$1.2M
NIGMS NIH HHS R35 GM128741NIH HHS R35GM128741-01
6 · The paper itself

Abstract

Photomediated Giese reactions are at the forefront of radical chemistry, much like the classical tin-mediated Giese reactions were nearly forty years ago. With the global recognition of organometallic photocatalysts for the mild and tunable generation of carbon-centered radicals, chemists have developed a torrent of strategies to form previously inaccessible radical intermediates that are capable of engaging in intermolecular conjugate addition reactions. This Review summarizes advances in photoredox-mediated Giese reactions since 2013, with a focus on the breadth of methods that provide access to crucial carbon-centered radical intermediates that can engage in radical conjugate addition processes.

Indexed as

CarbonFree RadicalsMolecular StructureOxidation-ReductionPhotochemical ProcessesCarbonFree RadicalsGiese reactionphotocatalysisphotoredox catalysisradical conjugate additionradical Michael addition

Identifiers

PMID33629454
PMCPMC8382814

What OpenQuestion holds

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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.