Skip to main content
SpringerLink
Log in

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:
Bulletin of Environmental Contamination and Toxicology Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  • 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

    Article  CAS  Google Scholar 

  • 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

    Article  CAS  Google Scholar 

  • 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

    Article  CAS  Google Scholar 

  • 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

    Article  CAS  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Chamberlain K, Carter GA (1980) The fungitoxicity of substituted 2-phenyl benzofurans. Pestic Sci 11: 526–532

    Article  CAS  Google Scholar 

  • Chen J, Wang L, Lu G, Zhao T (1997) Quantitative structure-activity relationships studies of selected heterocyclic nitrogen compounds. Bull Environ Contain Toxicol 58: 372–379

    Article  CAS  Google Scholar 

  • Chen R-Y, Wang H-L, Zhou J (1994) Synthesis and properties of novel amino acid linked phosphoryl nitrogen mustard derivatives. Heteroatom Chem 5: 497–501

    Article  CAS  Google Scholar 

  • Cremlyn RJW, David J, Kishore N (1974) The synthesis and fungicidal activity of derivatives of o and p-cyclohexylphenyl phosphorodichloridates and dichlorido-phosphorothioates. Pestic Sci 5: 667–673

    Article  CAS  Google Scholar 

  • Dureja P, Roy NK, Mukerjee SK (1980) Preparation and biocidal activity of alkyl phenyl (dichloromethyl) phosphonates. Pestic Sci 11: 685–688

    Article  CAS  Google Scholar 

  • Hansch C, Fujita T (1964) ρ-σ-π Analysis. A method for correlation of biological activity and chemical structure. J Am Chem Soc 86: 1616–1626

    Article  CAS  Google Scholar 

  • Hansch C, Leo A (1979) Substituent constants for correlation analysis in chemistry and biology. Wiley. New York

    Google Scholar 

  • Hassall KA (1990) The Biochemistry and uses of pesticides. 2nd Ed., Macmillan Press Ltd. Hong Kong

    Google Scholar 

  • Havis ND, Walters DR, Martin WP, Cook FM, Robins DJ (1996) Synthesis and fungicidal activity of alicyclic diamines. J Agric Food Chem 44: 2835- 2838

    Article  CAS  Google Scholar 

  • Ismail SMM, Ali HM, Habiba RA (1993) GC-ECD and GC-MS analysis of profenofos and its biochemical effects in tomato and tomato products. J Agric Food Chem 41: 610–615

    Article  CAS  Google Scholar 

  • Roy NK, Nidiry ESJ, Vasu K, Bedi S, Lalljee B, Singh B (1996) Quantitative structure-activity relationship studies of O, O-bisaryl alkyl phosphorate fungicides by Hansch approach and principal component analysis. J Agric Food Chem 44: 3971–3976

    Article  CAS  Google Scholar 

  • Swain CG, Unger SH, Rosenquist NR, Swain MS (1983) Substituent effects on chemical reactivity. Improved evaluation of field and resonance components. J Am Chem Soc 105: 492–502

    Article  CAS  Google Scholar 

  • Taft RW (1956) Steric Effects in Organic Chemistry. Wiley, New York

    Google Scholar 

  • Zhao YH, Wang LS, Gao H, Zhang Z (1993) Quantitative structure-activity relationships-Relationship between toxicity of organic chemicals to fish and to Photobacterium Phosphoreum. Chemosphere 26: 1971–1979

    Article  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Department of Agricultural Biochemistry, Faculty of Agriculture, Ain Shams University, 11241, Cairo, Egypt

    H. M. Ali

  2. Department of Plant Pathology, Faculty of Agriculture, Ain Shams University, 11241, Cairo, Egypt

    M. K. Ali

Authors
  1. H. M. Ali
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. M. K. Ali
    View author publications

    You can also search for this author in PubMed Google Scholar

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ali, H.M., Ali, M.K. 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. Bull. Environ. Contam. Toxicol. 65, 415–420 (2000). https://doi.org/10.1007/s001280000023

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s001280000023

Keywords

Search

Navigation