Results 231 to 240 of about 46,055 (292)
Interfacial proton-electron donor synergy enables sustainable oxime electrosynthesis via dual-path reduction. [PDF]
Wang S +8 more
europepmc +1 more source
Design, synthesis, and antifungal activity of anethole-based oxime ester compounds as potential laccase inhibitors. [PDF]
Bi Y +7 more
europepmc +1 more source
Flavonoid Oxime Carbamate Derivatives: Reversal of Multidrug Resistance in Cancer Cells. [PDF]
Barbosa F +5 more
europepmc +1 more source
Uranyl complexes with ligands possesing oxime or amidoxime groups
Στυλιανός Καρπούζης
openalex +1 more source
Chemical reaction rates are generally decreased at lower temperatures. Here, we report that an oxime ligation reaction in water at neutral pH is accelerated by freezing. The freezing method and its rate effect on oxime ligation are systematically studied on a peptide model system, and applied to a larger chemokine protein, containing a single acetyl ...
Agten, Stijn M. +2 more
openaire +3 more sources
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ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Albina I Mikhaleva +2 more
openaire +1 more source
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Albina I Mikhaleva +2 more
openaire +1 more source
Conversion of an oxime into the corresponding thio-oxime
Journal of the Chemical Society, Chemical Communications, 1976The thio-oximate anion derived from benzo-phenone oxime is prepared in solution by the action of sodium t-butoxide on N-diphenylmethylene-S-phenyl-carbamoylsulphimide, itself prepared by thermal rearrangement of the isomeric N-diphenylmethylene-O-phenylthiocarbamoylhydroxylamine.
Houshang Dj-Forudian +2 more
openaire +1 more source
2022
This chapter discusses the synthesis and properties of compounds with N-N bonds. It looks into the synthesis and reaction of hydrazines, hydrazides, hydrazones, diazo compounds, and azides. The N-N-containing functional groups undergo vital interconversions which have great synthetic value.
Patrick D. Bailey, Keith M. Morgan
openaire +1 more source
This chapter discusses the synthesis and properties of compounds with N-N bonds. It looks into the synthesis and reaction of hydrazines, hydrazides, hydrazones, diazo compounds, and azides. The N-N-containing functional groups undergo vital interconversions which have great synthetic value.
Patrick D. Bailey, Keith M. Morgan
openaire +1 more source

