Evidence map›Paper›PMID 38269039›Full record

ArticleACS catalysis2024

Organocatalytic Asymmetric Synthesis of Si-Stereogenic Siloxanols.

Jacob J Dalton, Adilene Bernal Sánchez, Austin T Kelly, James C Fettinger, Annaliese K Franz

Abstract read
In one paragraph

Article in ACS catalysis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Homologous Ladder Cyclohexasilanes.Angewandte Chemie (International ed. in English) · 2025
    Article
  2. Article
  3. Review
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

5 authors.

Jacob J DaltonDepartment of Chemistry, University of California Davis, One Shields Ave, Davis, California 95616, United States.
Adilene Bernal SánchezDepartment of Chemistry, University of California Davis, One Shields Ave, Davis, California 95616, United States.
Austin T KellyDepartment of Chemistry, University of California Davis, One Shields Ave, Davis, California 95616, United States.
James C FettingerDepartment of Chemistry, University of California Davis, One Shields Ave, Davis, California 95616, United States.ORCID https://orcid.org/0000-0002-6428-4909
Annaliese K FranzDepartment of Chemistry, University of California Davis, One Shields Ave, Davis, California 95616, United States.ORCID https://orcid.org/0000-0002-4841-2448

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We report the organocatalytic synthesis of Si-stereogenic compounds via desymmetrization of a prochiral silanediol with a chiral imidazole-containing catalyst. This metal-free silylation method affords high yields with enantioselectivity up to 98:2 for various silanediol and silyl chloride substrate combinations (including secondary alkyl, vinyl, and H groups), accessing products with potential for further elaboration. NMR and X-ray studies reveal insight into the H-bonding interactions between the imidazole organocatalyst and the silanediol and the dual activating role of the Lewis basic imidazole to account for the high enantioselectivity.

Identifiers

PMID38269039
PMCPMC10804373

What OpenQuestion holds

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Registered trials

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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.