Enantioselective Hydrogen Atom Relay via Non-covalent Catalyst Assembly

Enantioselective hydrogen atom transfer (HAT) has great synthetic potential, but the de novo design of chiral HAT catalysts is challenging. We report a conceptually distinct approach in which chiral HAT catalysts are generated in situ through non-covalent self-assembly of privileged chiral phosphoric acids and commercial 2-mercaptopyridines. The phosphoric acid serves as a modular chiral source that renders the achiral thiol effectively chiral, enabling a previously inaccessible combinatorial space of chiral HAT catalysts. This platform enabled the photochemical deracemization of 2-aryl pyrrolidines, a prevalent scaffold in active pharmaceutical ingredients. Optical enrichment proceeds via enantioselective hydrogen atom relay, in which a single chiral assembly orchestrates both hydrogen atom abstraction and delivery. This concept of relaying chiral information via non-covalent assembly holds broad potential for asymmetric radical catalysis.

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Publication Details

Journal
ChemRxiv
Published
2026-01-05
DOI
https://doi.org/10.26434/chemrxiv-2026-qwhqp
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
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article

Enantioselective Hydrogen Atom Relay via Non-covalent Catalyst Assembly

Giuseppe Zuccarello, Jules Hugo Alexandre, Navadheer Yalamanchili
ChemRxiv
Radical Photochemical Reactions
article

Enantioselective Hydrogen Atom Relay via Non-covalent Catalyst Assembly

Giuseppe Zuccarello, Jules Hugo Alexandre, Navadheer Yalamanchili
article en

Abstract

Enantioselective hydrogen atom transfer (HAT) has great synthetic potential, but the de novo design of chiral HAT catalysts is challenging. We report a conceptually distinct approach in which chiral HAT catalysts are generated in situ through non-covalent self-assembly of privileged chiral phosphoric acids and commercial 2-mercaptopyridines. The phosphoric acid serves as a modular chiral source that renders the achiral thiol effectively chiral, enabling a previously inaccessible combinatorial space of chiral HAT catalysts. This platform enabled the photochemical deracemization of 2-aryl pyrrolidines, a prevalent scaffold in active pharmaceutical ingredients. Optical enrichment proceeds via enantioselective hydrogen atom relay, in which a single chiral assembly orchestrates both hydrogen atom abstraction and delivery. This concept of relaying chiral information via non-covalent assembly holds broad potential for asymmetric radical catalysis.

ChemRxiv
École Polytechnique Fédérale de Lausanne (CH)
Openalex Percentile: Top 95%
Radical Photochemical Reactions
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