Evidence map›Paper›PMID 41703721›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Photoinduced Generation of (Boryl)Silyl and (Chloro)Silyl Radicals: Access to Trisubstituted Silylboranes and Chlorosilanes.

Mone Suzuki, Yuki Nagashima

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Mone SuzukiDepartment of Chemical Science and Engineering, Institute of Science Tokyo, Tokyo, Japan.
Yuki NagashimaGraduate School of Pharmaceutical Sciencesm, The University of Tokyo, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8470-5638

Funding

Asahi Glass FoundationJSPS Grant-in-Aid for Exploratory Research 24K21762JSPS Grants-in-Aid for Scientific Research 23H01956Transformative Research Areas 24H01067Transformative Research Areas 24H01839Uehara Memorial Foundation
6 · The paper itself

Abstract

Trisubstituted silylboranes and chlorosilanes are in high demand for the precise synthesis of tetrasubstituted organosilicons. However, conventional synthetic methods often require harsh conditions and exhibit low functional-group tolerance, limiting their chemical diversity. In this study, we present a versatile photoinduced hydro(boryl)silylation and hydro(chloro)silylation of alkenes to construct trisubstituted silylboranes and chlorosilanes. This method employs the in situ generation of novel silyl radicals, such as (boryl)silyl radicals (R

Indexed as

chlorosilaneshydrosilylationphotoinduced reactionssilylboranessilyl radicals

Identifiers

PMID41703721
PMCPMC13007590

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.