Stereoselective synthesis of flavonoids: A brief overview
AM Pereira, H Cidade, ME Tiritan - Molecules, 2023 - mdpi.com
Stereoselective synthesis has been emerging as a resourceful tool because it enables the
obtaining of compounds with biological interest and high enantiomeric purity. Flavonoids are …
obtaining of compounds with biological interest and high enantiomeric purity. Flavonoids are …
Flavones and related compounds: synthesis and biological activity
This review focuses on the synthesis and biological activity of flavones and their related
flavonoidic compounds, namely flavonols and aurones. Among the biological activities of …
flavonoidic compounds, namely flavonols and aurones. Among the biological activities of …
In memory of Prof. Venkataraman: Recent advances in the synthetic methodologies of flavones
R Kshatriya, VP Jejurkar, S Saha - Tetrahedron, 2018 - Elsevier
Flavones are present in a variety of medicines and natural products and are important
structural motif due to their unique mode of physiological action. Hence the structural …
structural motif due to their unique mode of physiological action. Hence the structural …
TaBr5-catalyzed Biginelli reaction: one-pot synthesis of 3, 4-dihydropyrimidin-2-(1H)-ones/thiones under solvent-free conditions
N Ahmed, JE van Lier - Tetrahedron letters, 2007 - Elsevier
An efficient TaBr5 (5–10mol%)-catalyzed Biginelli reaction under solvent-free conditions for
one-pot syntheses of 3, 4-dihydropyrimidin-2-(1H)-ones (DHPMs) and their thione analogs …
one-pot syntheses of 3, 4-dihydropyrimidin-2-(1H)-ones (DHPMs) and their thione analogs …
Ionic liquid mediated Cu-catalyzed cascade oxa-Michael-oxidation: efficient synthesis of flavones under mild reaction conditions
Z Du, H Ng, K Zhang, H Zeng, J Wang - Organic & Biomolecular …, 2011 - pubs.rsc.org
Flavonoids are a class of natural products, found in a wide range of vascular plants and
dietary components. Their low toxicity and extensive biological activities, including anti …
dietary components. Their low toxicity and extensive biological activities, including anti …
Diversity‐Oriented Approach to Biologically Relevant Molecular Frameworks Starting with β‐Naphthol and Using the Claisen Rearrangement and Olefin Metathesis as …
A diversity‐oriented approach for the synthesis of various structurally different molecular
frameworks from readily accessible and common precursors is described. A Claisen …
frameworks from readily accessible and common precursors is described. A Claisen …
Silica gel supported TaBr5: new catalyst for the facile and rapid cyclization of 2′-aminochalcones to the corresponding 2-aryl-2, 3-dihydroquinolin-4 (1H)-ones under …
N Ahmed, JE van Lier - Tetrahedron letters, 2006 - Elsevier
Silica gel supported TaBr5 (5–10mol%) is a new solid-support catalyst that can be used
under solvent-free conditions for the facile and efficient isomerization of 2 …
under solvent-free conditions for the facile and efficient isomerization of 2 …
InCl3: A Versatile Catalyst for Synthesizing a Broad Spectrum of Heterocycles
This review deals with the recent applications of the indium trichloride (InCl3) catalyst in the
synthesis of a broad spectrum of heterocyclic compounds. Over the years, a number of …
synthesis of a broad spectrum of heterocyclic compounds. Over the years, a number of …
Construction of the flavones and aurones through regioselective carbonylative annulation of 2-bromophenols and terminal alkynes
J Liu, M Liu, Y Yue, N Zhang, Y Zhang, K Zhuo - Tetrahedron Letters, 2013 - Elsevier
The easily available and efficient catalyst containing a benzimidazolium ligand and PdCl2
(PPh3) 2 demonstrated excellent catalytic activity to construct the flavones and aurones …
(PPh3) 2 demonstrated excellent catalytic activity to construct the flavones and aurones …
Alumina supported-CeCl3· 7H2O–NaI: an efficient catalyst for the cyclization of 2′-aminochalcones to the corresponding 2-aryl-2, 3-dihydroquinolin-4 (1H)-ones …
N Ahmed, JE van Lier - Tetrahedron Letters, 2007 - Elsevier
We recently advanced silica gel supported-TaBr5 as an efficient catalyst for the
isomerization of 2′-aminochalcones to the corresponding 2-aryl-2, 3-dihydroquinolin-4 …
isomerization of 2′-aminochalcones to the corresponding 2-aryl-2, 3-dihydroquinolin-4 …