Synthetic Routes to Coumarin(Benzopyrone)-Fused Five-Membered Aromatic Heterocycles Built on the α-Pyrone Moiety. Part II: Five-Membered Aromatic Rings with Multi Heteroatoms - Université de Lorraine Access content directly
Journal Articles Molecules Year : 2021

Synthetic Routes to Coumarin(Benzopyrone)-Fused Five-Membered Aromatic Heterocycles Built on the α-Pyrone Moiety. Part II: Five-Membered Aromatic Rings with Multi Heteroatoms

Abstract

Coumarins are natural heterocycles that widely contribute to the design of various biologically active compounds. Fusing different aromatic heterocycles with coumarin at its 3,4-position is one of the interesting approaches to generating novel molecules with various biological activities. During our continuing interest in assembling information about fused five-membered aromatic heterocycles, and after having presented mono-hetero-atomic five-membered aromatic heterocycles in Part I. The current review Part II is intended to present an overview of the different synthetic routes to coumarin (benzopyrone)-fused five-membered aromatic heterocycles with multi-heteroatoms built on the pyrone ring, covering the literature from 1945 to 2021.
Fichier principal
Vignette du fichier
molecules-2021 EE AB GK coumarins 2.pdf (5.76 Mo) Télécharger le fichier
Origin : Files produced by the author(s)

Dates and versions

hal-03372730 , version 1 (11-10-2021)

Licence

Attribution

Identifiers

Cite

Eslam Reda El-Sawy, Ahmed Bakr Abdelwahab, Gilbert Kirsch. Synthetic Routes to Coumarin(Benzopyrone)-Fused Five-Membered Aromatic Heterocycles Built on the α-Pyrone Moiety. Part II: Five-Membered Aromatic Rings with Multi Heteroatoms. Molecules, 2021, 26 (11), pp.3409. ⟨10.3390/molecules26113409⟩. ⟨hal-03372730⟩
25 View
74 Download

Altmetric

Share

Gmail Facebook X LinkedIn More