Synthesis and tautomerization study of pseudonitrosites to 1,2-nitroximes-Reference-Cited by-同舟云学术

Synthesis and tautomerization study of pseudonitrosites to 1,2-nitroximes

Published:2008-03-01 Issue:3 Volume:86 Page:248-252
ISSN:0008-4042
Container-title:Canadian Journal of Chemistry
language:en
Short-container-title:Can. J. Chem.

Author:

Shaabani Ahmad,Bijanzadeh Hamid Reza,Karimi Ali Reza,Teimouri Mohammad Bagher,Soleimani Kamal

Abstract

4-R-Substituted 2-nitro-1-nitrosoethylbenzenes (R = H, CH3, OCH3, Cl, F) have been synthesized under solvent-free conditions and the mechanism of their tautomerization to 2-isonitroso-1-nitro-2-phenylethanes have been investigated by 1H NMR spectroscopy.Key words: tautomerization, pseudonitrosite, mechanism, 2-nitro-1-nitrosoethylbenzene, 1H NMR spectroscopy

Publisher

Canadian Science Publishing

Subject

Organic Chemistry,General Chemistry,Catalysis

Link

http://www.nrcresearchpress.com/doi/pdf/10.1139/v08-011

Reference23 articles.

1. Preparations of C-Nitroso Compounds

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3. ACUTE NITROBENZOL POISONING WITH STUDIES ON THE BLOOD IN TWO CASES.*

4. Diethylaminoethyl 2,2-diphenylvalerate HCl (SKF 525-A)—In vivo and in vitro effects of metabolism by rat liver microsomes—Formation of an oxygenated complex

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