Reversed-polarity access to α-aminoketones using <i>in situ</i> generated siloxycarbenes from acylsilanes under photo-irradiation

Photo-induced addition reactions of acylsilanes, generating nucleophilic siloxycarbenes in situ , efficiently provide α -aminoketones from various imines.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-11-27
DOI
https://doi.org/10.1039/d5qo01438g
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
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article

Reversed-polarity access to α-aminoketones using in situ generated siloxycarbenes from acylsilanes under photo-irradiation

Organic Chemistry Frontiers
Radical Photochemical Reactions
article

Reversed-polarity access to α-aminoketones using in situ generated siloxycarbenes from acylsilanes under photo-irradiation

article en

Abstract

Photo-induced addition reactions of acylsilanes, generating nucleophilic siloxycarbenes in situ , efficiently provide α -aminoketones from various imines.

Organic Chemistry FrontiersVol. 13(3)
Seoul National University of Science and Technology (KR)
Openalex Percentile: Top 44%
Radical Photochemical Reactions
DOISourceOpenAlex
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Reversed-polarity access to α-aminoketones using <i>in situ</i> generated siloxycarbenes from acylsilanes under photo-irradiation · Organic Chemistry Frontiers (2025) | TGRS Research Map | TGRS