Issue 11, 2023

Hemicurcuminoids (1-styryl-1,3-diketones) – valuable multi-faceted building blocks for organic synthesis

Abstract

For the first time, a review has been conducted on the methods for the synthesis, as well as on the chemical, physical and biological properties, of 5-arylpent-4-ene-1,3-diones (hemicurcuminoids). The most prominent pathways for construction of the enedione moiety are the Pabon reaction, Baker–Venkataraman rearrangement and Claisen condensation. The obtained compounds could be used in the reactions with dinucleophiles, nucleophiles, and electrophiles or act as ambiphiles.

Graphical abstract: Hemicurcuminoids (1-styryl-1,3-diketones) – valuable multi-faceted building blocks for organic synthesis

Article information

Article type
Perspective
Submitted
31 aug 2022
Accepted
20 jan 2023
First published
24 jan 2023

New J. Chem., 2023,47, 5110-5149

Hemicurcuminoids (1-styryl-1,3-diketones) – valuable multi-faceted building blocks for organic synthesis

N. S. Zimnitskiy, V. Yu. Korotaev, A. Yu. Barkov, I. A. Kochnev and V. Ya. Sosnovskikh, New J. Chem., 2023, 47, 5110 DOI: 10.1039/D2NJ04338F

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