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Electrochemical Behavior of Aromatic N-Nitrosohydroxylamines

โœ Scribed by Elving, Philip J.; Olson, Edward C.

Book ID
127071176
Publisher
American Chemical Society
Year
1957
Tongue
English
Weight
938 KB
Volume
79
Category
Article
ISSN
0002-7863

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๐Ÿ“œ SIMILAR VOLUMES

N-nitrosohydroxylamines I. Acetolysis an
N-nitrosohydroxylamines I. Acetolysis and acid-catalyzed hydrolysis of N,O-dibenzyl-N-nitrosohydroxylamines. Reaction with potassium t-butoxide
โœ Kunio Kano; Jean-Pierre Anselme ๐Ÿ“‚ Article ๐Ÿ“… 1992 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 1004 KB

The major products of the hydrolysis of N,O-dibenzyl-N-nitrosohydroxylamines (3) are the denitrosated parent hydroxylamines (6); under mom forcing conditions, products of the further hydrolysis of 6 are obtained. Acetolysis in acetic acid gives the benzyl acetates derived from both N-and 0-substitue

The reaction of n,n-dibenzylcarbamoyl ch
The reaction of n,n-dibenzylcarbamoyl chloride with n-nitrosohydroxylamine
โœ Masayuki Nakajima; Jean-Pierre Anselme ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 119 KB

SUM!.4ARY: The action 06 N,N-dibenzy1tibamoyL ckeohide (21 on -the bodium da.& 06 N-niattobo-hy&oxy&minti (11 in dhy actiome at he&&ix .&&4 ti pmduc& whobe ,(otmati\_on may be trationaL&d in &amb 06 canbamoylatin aR e&heh oxygen 06 the bididen&zte N-tiobohy&oxy,kmi.mb.

Synthesis and tyrosinase inhibitory acti
Synthesis and tyrosinase inhibitory activity of novel N-hydroxybenzyl-N-nitrosohydroxylamines
โœ Mitsuhiro Shiino; Yumi Watanabe; Kazuo Umezawa ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 137 KB

Several novel N-substituted N-nitrosohydroxylamines were synthesized. They all inhibited mushroom tyrosinase, but the type of inhibition was different depending on the substituent. Some N-(mono- or dihydroxybenzyl)-N-nitrosohydroxylamines exhibited uncompetitive inhibition with respect to L-dopa. Am