Formation of ionized arylamines upon electron ionization of N-aryl-methyl-isoxazole-4-carboxamides: correlation with Hammett's constants and arylamine pKb's Mass spectra of arylmethylisoxazolecarboxamides-Reference-Cited by-同舟云学术

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Formation of ionized arylamines upon electron ionization of N-aryl-methyl-isoxazole-4-carboxamides: correlation with Hammett's constants and arylamine pKb's Mass spectra of arylmethylisoxazolecarboxamides

Published:2011-11 Issue:11 Volume:46 Page:1131-1134
ISSN:1076-5174
Container-title:Journal of Mass Spectrometry
language:en
Short-container-title:J. Mass. Spectrom.

Author:

Lee Chuan-Chen¹,Yang Ya-Chen¹,Lia Huei-Jia¹,Lin Shaw-Tao²

Affiliation:

1. Department of Health and Nutrition Biotechnology; Asia University; Wufeng; Taichung; 41354; Taiwan

2. Department of Applied Chemistry; Providence University; Sha-Lu; Taichung; 43301; Taiwan

Publisher

Wiley

Subject

Spectroscopy

Reference15 articles.

1. Cross-coupling reactions on azoles with two and more heteroatoms;Schnurch;Eur. J. Org. Chem.,2006

2. Recent advances on the synthesis and reactivity of isoxazoles;Pinho e Melo;Curr. Org. Chem.,2005

3. Leflunomide analogues as potential antiinflammatory agents;Huang;Chem. Pharm. Bull.,2003

4. Single- and multiple-dose pharmacokinetics and pharmacodynamics of leflunomide's active metabolite A77 1726 in normal Lewis rats;Silva;Transplant. Proc.,1996

5. Leflunomide and malononitrilamides;Silva;Am. J. Med. Sci.,1997

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1. Substituent Effect on the Tautomerization of 1-Arylazonaphthalen-2-ols by Mass Spectrometric Analysis;Journal of the Chinese Chemical Society;2015-02-13

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