Evidence map›Paper›PMID 42842655›Full record

ArticleScience advances2026

Optical resolution of H/D isotopic chirality via asymmetric C-H amination.

Tatsuya Uchida, Yuta Nakagawa, Naoki Watari, Yuuya Kawasaki

Abstract read
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Article in Science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Tatsuya UchidaDepartment of Chemistry, Graduate School of Sciences, Kyushu University; Fukuoka, 819-0395, Japan.ORCID 0000-0002-6511-5752
Yuta NakagawaDepartment of Chemistry, Graduate School of Sciences, Kyushu University; Fukuoka, 819-0395, Japan.ORCID 0009-0009-3858-7007
Naoki WatariDepartment of Chemistry, Graduate School of Sciences, Kyushu University; Fukuoka, 819-0395, Japan.
Yuuya KawasakiInstitute for Materials Chemistry and Engineering, Kyushu University, Kasuga, Fukuoka 816-8580, Japan.ORCID 0000-0003-3354-1690

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Isotopic chirality arising from hydrogen/deuterium substitution has long resisted optical resolution because isotopic substitution introduces only minimal stereochemical differences, rendering such molecules structurally pseudo-achiral. Recognizing that the small yet distinct difference in C-H/C-D bond dissociation energies (BDEs) creates an energetic asymmetry, we envisioned that an enantioselective C-H functionalization exploiting this disparity could achieve the kinetic resolution of isotopically chiral molecules. Here, we report a catalytic method for the optical resolution of benzylic and allylic H/D isotopic chirality. This method achieved a remarkably high separation factor (

Identifiers

PMID42842655
PMCPMC13644751

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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.