Enantioselective Copper-Catalyzed Synthesis of Hydroxylamines via Hydrofunctionalization of Alkenes using Nitroalkanes. [PDF]
Law JA +7 more
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TiCl<sub>3</sub>-Mediated Reductive Aminohydroxylation of Alkenes to (Benzo)Furo[3,2-<i>b</i>]Indolines. [PDF]
Boyarskaya D +4 more
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Association between Salted Seafood Consumption and Biliary Tract Cancer in Patients Living in the Island Regions of Tokyo: Ecological Study Using Population-based Cancer Registry Data. [PDF]
Okamoto E, Ito Y, Terada S, Fujiwara T.
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Identification of an Activity Selector for the Nitroso-Forming Activity in Bacterial Type-III Copper Enzymes. [PDF]
Le Xuan H, Panis F, Rompel A.
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Comprehensive Assessment of Nitrosamine Formation in Meat Products Using UHPLC-HRMS: Analytical Challenges and Potential Dietary Implications. [PDF]
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Sustainability in Analytical Chemistry Illustrated by Pharmaceutical Nitrosamine Testing. [PDF]
Bredendiek F, Schmidtsdorff S, Parr MK.
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Gut microbiota and diet in colorectal cancer: Converging determinants of carcinogenesis. [PDF]
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Reductive dominance and limited cytochrome P450 activity in neonicotinoid metabolism by elephant liver microsomes. [PDF]
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N-Nitroso compounds in the diet
Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 1999N-Nitroso compounds were known almost 40 years ago to be present in food treated with sodium nitrite, which made fish meal hepatotoxic to animals through formation of nitrosodimethylamine (NDMA). Since that time, N-nitroso compounds have been shown in animal experiments to be the most broadly acting and the most potent group of carcinogens.
W Lijinsky, William Lijinsky
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This chapter looks into the synthesis and reactions of N-oxides. The N-heteroatom bond of N-oxides is not introduced intact in the synthesis of compounds. However, it is delivered in an oxidation reaction. It notes peracid as the usual oxidant which is either used directly or generated in place from a carboxylic acid or hydrogen peroxide mixture.
Patrick D. Bailey, Keith M. Morgan
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