A Formal 1,2-Stevens Rearrangement of Thioester Ylides as a Single-Atom Molecular Editing Tool

A rhodium-catalyzed reaction of thioesters with diazo reagents was recognized as a powerful and unprecedented tool for single-atom molecular editing by the insertion of a single carbon atom into the C(O)─S thioester bond, thereby leading to various α-thioketones possessing a quaternary carbon atom. A selective and precise defunctionalization of the polyfunctionalized products further demonstrated the synthetic utility of the reaction for the synthesis of more common structural classes of compounds.

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Publication Details

Journal
Organic Letters
Published
2024-12-23
DOI
https://doi.org/10.1021/acs.orglett.4c04495
Citations
4
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.00

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article

A Formal 1,2-Stevens Rearrangement of Thioester Ylides as a Single-Atom Molecular Editing Tool

Filip Bihelović, Zorana Ferjančić, Ivan Borkovic
4 citations
Organic Letters
Catalytic C–H Functionalization Methods
1.00
article

A Formal 1,2-Stevens Rearrangement of Thioester Ylides as a Single-Atom Molecular Editing Tool

Filip Bihelović, Zorana Ferjančić, Ivan Borkovic
article en
4 citations

Abstract

A rhodium-catalyzed reaction of thioesters with diazo reagents was recognized as a powerful and unprecedented tool for single-atom molecular editing by the insertion of a single carbon atom into the C(O)─S thioester bond, thereby leading to various α-thioketones possessing a quaternary carbon atom. A selective and precise defunctionalization of the polyfunctionalized products further demonstrated the synthetic utility of the reaction for the synthesis of more common structural classes of compounds.

Organic LettersVol. 27(1)
University of Belgrade (RS)
Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja, Science Fund of the Republic of Serbia
Zero hunger
Openalex Percentile: Top 26%
Catalytic C–H Functionalization Methods
1.00
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