𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The reaction of n,n-dibenzylcarbamoyl chloride with n-nitrosohydroxylamine

✍ Scribed by Masayuki Nakajima; Jean-Pierre Anselme

Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
119 KB
Volume
25
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis

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.

πŸ“œ SIMILAR VOLUMES

The Reaction of N,N-Dibenzylcarbamoyl Ch
The Reaction of N,N-Dibenzylcarbamoyl Chloride with Silver Nitrate
✍ Masayuki Nakajima; Jean-Pierre Anselme πŸ“‚ Article πŸ“… 2010 πŸ› Wiley (John Wiley & Sons) βš– 86 KB πŸ‘ 2 views

The reaction of disubstituted carbamoyl chlorides and sulfamoyl chlorides with sodium nitrite in acetonitrile has been shown to afford N-nitrosamines in excellent yields. In 1959, Norris had described the reaction of dialkylcarbamoyl chlorides with silver nitrate: mixtures of dialkylnitramines and

N-nitrosohydroxylamines I. Acetolysis an
N-nitrosohydroxylamines I. Acetolysis and acid-catalyzed hydrolysis of N,O-dibenzyl-N-nitrosohydroxylamines. Reaction with potassium t-butoxide
✍ Kunio Kano; Jean-Pierre Anselme πŸ“‚ Article πŸ“… 1992 πŸ› Elsevier Science 🌐 French βš– 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