One-pot sequential synthesis of O-(halo-substituted benzyl) hydroxylammonium salts
In this study, we described a simple one-pot preparation of O-(halo-substituted benzyl) hydroxylamine derivatives by O-benzylation of N-hydroxyurethane, followed by basic N-deprotection. The advantages of the method were the chemo- and regio-selectivity in obtaining the desired O-benzyl hydroxylammo...
Main Authors: | Saeed Emami, Alireza Foroumadi |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2017-02-01
|
Series: | Arabian Journal of Chemistry |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1878535212001852 |
Similar Items
-
Preparation of N-Substituted Hydroxylamines from Oxaziridines
by: Truitt, Sharon G.
Published: (1968) -
Manufacture of hydroxylamine by reduction of nitric oxide in trickle-bed electrochemical reactors
by: Bathia, Mahendra Liladhar
Published: (2010) -
Applications of the reverse Cope elimination
by: Cleator, Edward
Published: (2001) -
Nitrate ammonification by Nautilia profundicola AmH: experimental evidence consistent with a free hydroxylamine intermediate.
by: Thomas E Hanson, et al.
Published: (2013-07-01) -
Hydroxylammonium Tetrafluoridooxidovanadate(V) – (NH3OH)[VOF4]
by: Matic Lozinšek
Published: (2015-05-01)