نتایج جستجو برای: substituted nitrile oxide

تعداد نتایج: 216363  

2017
Hideji Tanii

OBJECTIVES Allyl nitrile (3-butenenitrile) occurs naturally in the environment, in particular, in cruciferous vegetables, indicating a possible daily intake of the compound. There is no report on actual health effects of allyl nitrile in humans, although it is possible that individuals in the environment are at a risk of exposure to allyl nitrile. However, little is known about its quantitative...

Journal: :iranian journal of catalysis 2014
tarlan salehi-hamzehkhani marzieh hatami abdolkarim zare ahmad reza moosavi-zare abolfath parhami

michael addition of pyrimidine and purine nucleobases to substituted as well as unsubstituted α,β-unsaturated esters efficiently proceeds in the presence of catalytic amount of zinc oxide in ionic liquid 1-butyl-3-methylimidazolium bromide (zno/[bmim]br) under microwave irradiation to afford carboacyclic nucleosides, as biologically important compounds, in good to excellent yields and in short ...

Journal: :Organic & biomolecular chemistry 2012
Melissa L McIntosh Michael R Naffziger Bradley O Ashburn Lev N Zakharov Rich G Carter

The dipolar cycloadditions of ortho-nitrophenyl alkynes with aryl nitrile oxides has been demonstrated. A range of substituents are tolerated on the alkyne. These reactions proceed with excellent levels of regioselectivity. Subsequent functionalization of the isoxazole scaffold has been demonstrated.

Journal: :The Biochemical journal 2000
E R Werner H J Habisch A C Gorren K Schmidt L Canevari G Werner-Felmayer B Mayer

Tetrahydrobiopterin [(6R)-5,6,7,8-tetrahydro-L-biopterin, H(4)biopterin] is one of several cofactors of nitric oxide synthases (EC 1.14.13.39). Here we compared the action of N(5)-substituted derivatives on recombinant rat neuronal nitric oxide synthase with their effects on dihydropteridine reductase (EC 1.6.99.7) and phenylalanine hydroxylase (EC 1.14.16.1),the well-studied classical H(4)biop...

2012
Alan O. Marron Michael Akam Giselle Walker

BACKGROUND Nitrile hydratases are enzymes involved in the conversion of nitrile-containing compounds into ammonia and organic acids. Although they are widespread in prokaryotes, nitrile hydratases have only been reported in two eukaryotes: the choanoflagellate Monosiga brevicollis and the stramenopile Aureococcus anophagefferens. The nitrile hydratase gene in M. brevicollis was believed to have...

Journal: :The Journal of biological chemistry 2013
Natalie Gumataotao Misty L Kuhn Natalia Hajnas Richard C Holz

Stopped-flow kinetic data were obtained for the iron-type nitrile hydratase from Rhodococcus equi TG328-2 (ReNHase) using methacrylonitrile as the substrate. Multiple turnover experiments suggest a three-step kinetic model that allows for the reversible binding of substrate, the presence of an intermediate, and the formation of product. Microscopic rate constants determined from these data are ...

Journal: :European Journal of Organic Chemistry 2021

Novel lupane-type triterpenoid-isoxazole conjugates were designed by direct placing of isoxazole linker at C(17) triterpenoid. The suggested synthetic sequence demonstrates successful combination electro-organic synthesis and conventional approaches. TEMPO-mediated electrooxidation betulin to betulinal was developed optimized boron-doped diamond anodes with potassium acetate as inexpensive supp...

Journal: :Molecules 2017
Steve Scheiner

Heterodimers are constructed containing imidazolium and its halogen-substituted derivatives as Lewis acid. N in its sp³, sp² and sp hybridizations is taken as the electron-donating base. The halogen bond is strengthened in the Cl < Br < I order, with the H-bond generally similar in magnitude to the Br-bond. Methyl substitution on the N electron donor enhances the binding energy. Very little per...

Journal: :Journal of the American Chemical Society 2002
Juventino J Garcia Nicole M Brunkan William D Jones

The nickel(0) fragment [(dippe)Ni] has been found to react with a variety of aromatic nitriles. Initial pi-coordination to the C=C and Ctbd1;N bonds of 2-cyanoquinoline is found to lead ultimately to C-CN oxidative addition. 3-Cyanoquinoline reacts similarly, although no eta(2)-CN complex is observed. 2-, 3-, And 4-cyanopyridines react initially to give eta(2)-nitrile complexes that then lead t...

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