-C = କ any ଣସି ଯ ound ଗିକ ଗୋଷ୍ଠୀ ଧାରଣ କରିଥିବା ନୋହ |,

oximes's Usage Examples:

ethylenimine synthesis is a method for constructing ethyleneimines from oximes.

Progesterone dioxime Progestogen ester § Progestogen oximes List of progestogen esters § Oximes of progesterone derivatives Progesterone (medication).

norelgestromin and the non-marketed progestin norethisterone acetate oxime, are C3 oximes, although they have potent progestogenic activity of their own and are not.

as the chloride or iodide salts, belongs to a family of compounds called oximes that bind to organophosphate-inactivated acetylcholinesterase.

phosphaalkynes, isocyanides, carbon monoxide, dinitrogen, nitriles, cyanamides, nitric oxide, oximes, oxadiazolines, carboxamides, amidines, olefins.

compounds called oximes that bind to organophosphate-inactivated acetylcholinesterase.

progestogen oximes have not been marketed: EIDD-036 (progesterone 20-oxime; P4-20-O) EIDD-1723 (progesterone 20E-[O-[(phosphonooxy)methyl]oxime] sodium salt).

Oxidation of oximes and primary amines to nitro compounds Glycol cleavage Oxidative cleavage of α-Hydroxy acids Alkene oxidations Oxidation of primary amines.

propionaldehyde; Corvinan, Delvosteron) Although not esters, the following progestogen oximes have not been marketed: EIDD-036 (progesterone 20-oxime; P4-20-O) EIDD-1723.

Amidoximes are oximes of amides with general structure R1C(NOH)NR2R3.

palladium-on-carbon Iron metal Lithium aluminium hydride (Note: Hydroxylamines and oximes are typical impurities.