Quantitative structure-activity relationships (QSAR) of two series of O-aryl or N-aryl O-ethyl phosphoramidate and phosphorodiamidate fungicides incorporating amino acid ethyl esters-Reference-Cited by-同舟云学术

Quantitative structure-activity relationships (QSAR) of two series of O-aryl or N-aryl O-ethyl phosphoramidate and phosphorodiamidate fungicides incorporating amino acid ethyl esters

Published:2000-10 Issue:4 Volume:65 Page:415-420
ISSN:0007-4861
Container-title:Bulletin of Environmental Contamination and Toxicology
language:en
Short-container-title:Bull. Environ. Contam. Toxicol.

Author:

Ali H. M.,Ali M. K.

Publisher

Springer Science and Business Media LLC

Subject

Health, Toxicology and Mutagenesis,Pollution,Toxicology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s001280000023.pdf

Reference19 articles.

1. Ali HM, Mohamed KA (1999) Synthesis and quantitative structure-activity relationship of a new series of chiral 4-alkoxycarbonyl-2-(alkylamino)-1,3,2- oxa or thiazaphospholidine-2-ones. Hetroatom Chem 10: 475–480

2. Ali HM, Mostafa AA (1999) Quantitative structure-activity relationship of a series of N-aryl O-aryl phosphoramidate insecticides. Environ Toxicol Chem 18: 167–171

3. Ali HM, Mostafa AA, El-Zohry MF (1999) Synthesis and bioactivity of O-ethyl phosphorodiamidates derived from quinazolin-4-ones and either amino acid esters or fatty amines. Hetroatom Chem 10: 455–460

4. Andersen RA, Hamilton-Kemp TR, Hildebrand DF, McCracken CT, Jr, Collins RW, Fleming PD (1994) Structure-antifungal activity relationships among volatile C6 and C9 aliphatic aldehydes, ketones, and alcohols. J Agric Food Chem 42: 1563–1568

5. Bravo HR, Lazo W (1996) Antialgal and antifungal activity of natural hydroxamic acids and related compounds. J Agric Food Chem 44: 1569- 1571.

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