TY - JOUR

T1 - Hemicurcuminoids (1-styryl-1,3-diketones) – valuable multi-faceted building blocks for organic synthesis

AU - Zimnitskiy, Nikolay S.

AU - Korotaev, Vladislav Yu.

AU - Barkov, Alexey Yu.

AU - Kochnev, Ivan A.

AU - Sosnovskikh, Vyacheslav Ya.

N1 - The research funding from the Ministry of Science and Higher Education of the Russian Federation (Ural Federal University Program of Development within the Priority-2030 Program) is gratefully acknowledged.

PY - 2023

Y1 - 2023

N2 - 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.

AB - 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.

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000937202600001

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85149259577

U2 - 10.1039/D2NJ04338F

DO - 10.1039/D2NJ04338F

M3 - Review article

VL - 47

SP - 5110

EP - 5149

JO - New Journal of Chemistry

JF - New Journal of Chemistry

SN - 1144-0546

IS - 11

ER -