Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Nitroacetic acid"'
Autor:
Gianfranco Ercolani, Daniele Del Giudice, Cecilia Bombelli, Emanuele Spatola, M. Valentini, Stefano Di Stefano
Publikováno v:
Chemical Science
In this report it is shown that nitroacetic acid 1 (O2NCH2CO2H) can be conveniently used to control the pH of a water solution over time. Time-programmable sequences of the kind pH1(high)–pH2(low)–pH3(high) can be achieved, where both the extent
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Autor:
Rose A. Pesce-Rodriguez, Jesse J. Sabatini, Eric C. Johnson, Pablo E. Guzmán, Leah A. Wingard
Publikováno v:
Organic Process Research & Development. 21:1088-1090
A new procedure for the synthesis and isolation of methyl nitroacetate is described. The previously published method required drying the explosive dipotassium salt of nitroacetic acid in a vacuum desiccator, followed by grinding this material into a
Publikováno v:
Environmental Pollution. 261:114127
Pharmaceutical compounds at trace concentrations are found in the environment, especially in drinking water and food, posing significant negative effects on humans as well as on animals. This paper aimed to examine the diagnostic catalytic properties
Publikováno v:
Russian Journal of General Chemistry. 83:1764-1770
The method for preparation of ethyl α-nitrocinnamates by nitroacetic acid ester alkenylation with aromatic aldehydes in the presence of acetic acid and β-alanine has been modified. Structures of the prepared compounds have been proved by electronic
Autor:
Bethany Halford
Publikováno v:
C&EN Global Enterprise. 95:8-9
Methyl nitroacetate is a handy chemical building block. It can be used to produce α-amino acids, isoxazoles, and α,β-unsaturated compounds. It’s also a useful reactant in Michael additions, Mannich reactions, and cyclopropanations. But it’s ex
Autor:
Hiromu Kawakubo
Publikováno v:
Pharmaceutical Process Chemistry
Publikováno v:
Organic Letters. 4:497-500
[reaction: see text] Enantiomerically pure N-tosyl-2,3-aziridine alcohols are directly converted into 4-hydroxy-4,5-dihydroisoxazole 2-oxides through oxidation to the corresponding aldehydes followed by in situ tandem nitroaldol-intramolecular cycliz
Publikováno v:
Organicbiomolecular chemistry. 12(24)
A domino nitrosation and addition–elimination of nitroacetanilides with NaNO2 and H2SO4 has been developed to synthesize a variety of 1,4,2,5-dioxadiazine-3,6-dicarboxamides in excellent yields. The substrate scope can be extended to aryl nitrometh
Publikováno v:
Current Organic Chemistry. 5:553-570