Evidence map›Paper›PMID 41661000›Full record

ArticleJournal of the American Chemical Society2026

Switching Shapes: Reversible Three Species Photoisomerization of Substituted 1,2-Dihydro-1,2-azaborinines.

Sonja M Biebl, Jonas N Lienert, Adrian J Müller, Markus Ströbele, Andreas Dreuw, Josef Wachtveitl, Holger F Bettinger

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 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. Modular and Stereoselective Synthesis of Cyclobutane β-Amino Alcohols.Angewandte Chemie (International ed. in English) · 2026
    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

7 authors.

Sonja M BieblInstitut für Organische Chemie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany.ORCID 0000-0001-5489-4570
Jonas N LienertInstitut für Physikalische und Theoretische Chemie, Goethe-Universität Frankfurt, Max von Laue-Straße 7, 60438 Frankfurt am Main, Germany.
Adrian J MüllerInterdisciplinary Center for Scientific Computing, Heidelberg University, Im Neuenheimer Feld 205, 69120 Heidelberg, Germany.ORCID 0009-0008-8482-4790
Markus StröbeleInstitut für Anorganische Chemie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany.ORCID 0000-0002-5147-5677
Andreas DreuwInterdisciplinary Center for Scientific Computing, Heidelberg University, Im Neuenheimer Feld 205, 69120 Heidelberg, Germany.ORCID 0000-0002-5862-5113
Josef WachtveitlInstitut für Physikalische und Theoretische Chemie, Goethe-Universität Frankfurt, Max von Laue-Straße 7, 60438 Frankfurt am Main, Germany.ORCID 0000-0002-8496-8240
Holger F BettingerInstitut für Organische Chemie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany.ORCID 0000-0001-5223-662X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Derivatives of 1,2-dihydro-1,2-azaborinines generally undergo selective photochemical electrocyclic ring-closure reactions to the corresponding Dewar isomers (2-aza-3-borabicyclo[2.2.0]hex-5-ene). Depending on the substitution pattern, these photoreactions can also yield benzvalene (3-aza-4-boratricyclo[3.1.0.0

Identifiers

PMID41661000
PMCPMC13003484

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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.