Evidence map›Paper›PMID 42619107›Full record

ArticleJournal of the American Chemical Society2026

The Catalytic Enantioselective Sommelet-Hauser Rearrangement.

Ihssane El Fdali, Jacqueline M Laddusaw, Kevin Kasten, Aidan P McKay, David B Cordes, Paul Ha-Yeon Cheong, Andrew D Smith

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. Not yet cited in PubMed.

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

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

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

7 authors.

Ihssane El FdaliEaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St AndrewsKY16 9ST, United Kingdom.
Jacqueline M LaddusawDepartment of Chemistry, Oregon State University, 153 Gilbert Hall, Corvallis, Oregon97331, United States.
Kevin KastenEaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St AndrewsKY16 9ST, United Kingdom.ORCID 0000-0003-1298-8784
Aidan P McKayEaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St AndrewsKY16 9ST, United Kingdom.ORCID 0000-0002-8578-7054
David B CordesEaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St AndrewsKY16 9ST, United Kingdom.ORCID 0000-0002-5366-9168
Paul Ha-Yeon CheongDepartment of Chemistry, Oregon State University, 153 Gilbert Hall, Corvallis, Oregon97331, United States.
Andrew D SmithEaStCHEM, School of Chemistry, University of St Andrews, North Haugh, St AndrewsKY16 9ST, United Kingdom.ORCID 0000-0002-2104-7313

Funding

Division of Chemistry CHE-2454071Engineering and Physical Sciences Research Council (EPSRC) EP/T023643/1Engineering and Physical Sciences Research Council (EPSRC) EP/W007517Ohio State University NAUK Research and Innovation (UKRI) UKRI381
6 · The paper itself

Abstract

The Sommelet-Hauser rearrangement of ammonium ylides incorporates a dearomatizing [2,3]-sigmatropic rearrangement of a (hetero)aromatic substituent, followed by tautomerization (rearomatization), to generate (hetero)benzylic amine derivatives. Despite widespread interest in this process, asymmetric variants have previously relied upon stoichiometric chiral auxiliary or chirality transfer strategies to induce stereocontrol. In this manuscript, the organocatalytic enantioselective Sommelet-Hauser rearrangement of ammonium ylides bearing heteroaromatic substituents is demonstrated using a Lewis basic isothiourea catalyst, providing a series of unnatural α-heteroaryl α-amino acid derivatives with high to excellent enantioselectivity (up to 98:2 er). The developed process tolerates cyclic and acyclic ammonium salt precursors with indolyl and benzofuranyl substituents. A range of pronucleophiles was employed that lead to amide, ester, and alcohol products. Computational analysis revealed that a stepwise process (involving initial C-N bond cleavage to generate an ion pair, followed by a barrierless C-C bond formation) is favored over a concerted [2,3]-rearrangement, with distortion-interaction analysis providing insight into the factors that govern the mechanism. Crossover experiments, including the use of isotopologue salt derivatives to minimize chemical differentiation of substrates, showed no scrambling. The totality of accumulated computational and experimental evidence suggests a stepwise rearrangement involving a near-instantaneous second recombination step such that the overall process is indistinguishable from, and effectively, a concerted asynchronous rearrangement.

Identifiers

PMID42619107
PMCPMC13495760

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