Issue 28, 2020

Short and modular synthesis of tetraarylsalicylaldehydes

Abstract

In this study, we describe a novel strategy that allows the obtention of all 15 possible substitution geometries of perarylated salicylaldehydes with total control of the regioselectivity. This strategy entitles the formation of the salicylaldehyde core via a Claisen rearrangement of propargyl vinyl ethers, followed by bromination and Pd-catalyzed aryl–aryl cross-coupling reactions.

Graphical abstract: Short and modular synthesis of tetraarylsalicylaldehydes

Supplementary files

Article information

Article type
Communication
Submitted
28 Jan 2020
Accepted
02 Mar 2020
First published
05 Mar 2020
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2020,56, 4019-4022

Short and modular synthesis of tetraarylsalicylaldehydes

D. Tejedor, S. Delgado-Hernández, B. Santamaría-Peláez and F. García-Tellado, Chem. Commun., 2020, 56, 4019 DOI: 10.1039/D0CC00738B

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