Masked formylation of activated aromatics <i>via</i> dithianes and a mild, sustainable cleavage protocol

Masked formylation using dithiane oxide activated by oxalyl chloride via a thionium ion. It enables efficient substitution in electron-rich arenes and mild dithiane cleavage to aldehydes, offering a simple, versatile alternative to classical methods.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-10-17
DOI
https://doi.org/10.1039/d5qo01300c
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00
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article

Masked formylation of activated aromatics via dithianes and a mild, sustainable cleavage protocol

Diego Gamba‐Sánchez, Mario A. Macías, Camilo Mahecha‐Mahecha, Julia Urbiña-Alvarez et al.
Organic Chemistry Frontiers
Asymmetric Hydrogenation and Catalysis
article

Masked formylation of activated aromatics via dithianes and a mild, sustainable cleavage protocol

Diego Gamba‐Sánchez, Mario A. Macías, Camilo Mahecha‐Mahecha, Julia Urbiña-Alvarez, Daniela Torres-Ruiz, Gabriel Hernandez-Abdallah
article en

Abstract

Masked formylation using dithiane oxide activated by oxalyl chloride via a thionium ion. It enables efficient substitution in electron-rich arenes and mild dithiane cleavage to aldehydes, offering a simple, versatile alternative to classical methods.

Organic Chemistry FrontiersVol. 13(1)
Universidad de Los Andes (CO), Laboratoire de Synthèse Organique (FR)
Openalex Percentile: Top 75%
Asymmetric Hydrogenation and Catalysis
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