Tautomerism and isotopic multiplets in the 13 C NMR spectra of partially deuterated 3-arylpyrimido[4,5-c ]pyridazine-5,7(6H ,8H )-diones and their sulfur analogs-evidence for elucidation of the structure backbone and tautomeric forms-Reference-Cited by-同舟云学术

Tautomerism and isotopic multiplets in the 13 C NMR spectra of partially deuterated 3-arylpyrimido[4,5-c ]pyridazine-5,7(6H ,8H )-diones and their sulfur analogs-evidence for elucidation of the structure backbone and tautomeric forms

Published:2010-02-18 Issue:4 Volume:48 Page:276-285
ISSN:0749-1581
Container-title:Magnetic Resonance in Chemistry
language:en
Short-container-title:Magn. Reson. Chem.

Author:

Rimaz Mehdi,Noroozi Pesyan Nader,Khalafy Jabbar

Funder

Urmia University Research Council

Publisher

Wiley

Subject

General Materials Science,General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mrc.2573/fullpdf

Reference57 articles.

1. Pyrimidines and their Benzo Derivatives

2. Uracils: Versatile Starting Materials in Heterocyclic Synthesis

3. Inhibition of Monoamine Oxidase-B by Condensed Pyridazines and Pyrimidines: Effects of Lipophilicity and Structure−Activity Relationships

4. 6,8-Dimethylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-dione: new heterocyclizations based on SNH-methodology. Unexpected formation of the first iso-π-electronic analogue of the still unknown dibenzo[a,o]pycene

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