Free radical chemistry: A new approach to synthesis
نویسنده
چکیده
Introduction One of the long-term objectives of our research program is to contribute at strategic, tactical and theoretical levels with approaches leading to the creation of new stereogenic centers, notably on acyclic molecules, which as a class are among the most difficult chemical entities to transform stereoselectively due to their flexibility. Of particular interest to us is the use of free-radical intermediates that were completely overlooked in such approaches, until a decade ago. The synthesis of new biologically important molecules to be used in deciphering the mechanism of various biological processes or in interfering with a given pathology, is an equally important long-term objective of our laboratory, particularly we are interssested in the natural products derived from the polyketide biosynthesis pathway.
منابع مشابه
Investigation of dibromo and N-bromoacetyl derivatives of [b] carbazole-synthesis and antibacterial evaluation
The synthesis, structure and biological activity of carbazole compounds has been long focus of research interests in the field of medicinal chemistry. 5,8-dibromo-5,6-dihydro(3,2-a)carbazole A have prepared in good yield by a free radical bromination reaction of 8-bromo-5,6-dihydro9(3,2-a)carbazole with N-bromosuccinimide in carbontetrachloride at ambient temperature.. Compound 2 have prepared ...
متن کاملNew method for preparation of MWCNT-SO3H as an efficient and reusable catalyst for the solvent-free synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones
Multiwalled carbon nanotubes (MWCNTs) have been functionalized with -SO3H groups using new three steps chemical routes. Firstly, OH groups have been attached to CNT surfaces through a radical reaction. The second step involves converting the hydroxyl groups into the oxide one and last step included the attachment of –SO3H groups on the MWCNTs surfaces in the presence of 1-butyl-3-methyl imidazo...
متن کاملNew method for preparation of MWCNT-SO3H as an efficient and reusable catalyst for the solvent-free synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones
Multiwalled carbon nanotubes (MWCNTs) have been functionalized with -SO3H groups using new three steps chemical routes. Firstly, OH groups have been attached to CNT surfaces through a radical reaction. The second step involves converting the hydroxyl groups into the oxide one and last step included the attachment of –SO3H groups on the MWCNTs surfaces in the presence of 1-butyl-3-methyl imidazo...
متن کاملSynthesis of Polyvinyltetrazole by Combination of Free Radical Polymerization and Click Chemistry for Adsorption of Pb (II) in Aqueous Solution
Polyvinyltetrazole (PVT) is produced from acrylonitrile (AN) monomer by using free-radicalpolymerization and Click Chemistry methods. The resulting polymer with a broad range of tetrazolegroup contents was conveniently synthesized through [3+ 2] azide-nitrile cycloaddition reaction ofnitrile-containing polymer with sodium azide in DMF. The prepared PVT was characterized by13CN...
متن کاملDesign and synthesis of new esters of terpenoid alcohols as 15-lipoxygenase inhibitors
Objective(s): 15-Lipoxygenases are one of the iron-containing proteins capable of performing peroxidation of unsaturated fatty acids in animals and plants. The critical role of enzymes in the formation of inflammations, sensitivities, and some cancers has been demonstrated in mammals. The importance of enzymes has led to the development of mechanistic studies, product analysis, and synthesis of ...
متن کاملA simplified green approach for synthesis of arylquinoxalines under solvent-free clay-catalysed conditions
A friendly benign, green, rapid and facile strategy for synthesis a series of arylquinoxalines was achieved by condensation of aromatic 1,2-diamines with arylglyoxals under clay-catalyzed as an inexpensive and eco-friendly catalyst using grindstone chemistry. Significant decreases in reaction times and high yields have been observed by this green chemistry approach in comparison with previously...
متن کامل