Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/22370
Title: Synthesis and bioefficacy evaluation of 2-[4-(3-arylprop-2-enoyl)phenoxy]N- substituted acetamides and 2-[4-(5-aryl-4,5-dihydro-1H-pyrazol-3-yl)phenoxy] acetic acid hydrazides as potential pesticides
Authors: Malik, Heetika
Dahiya, Anjula
Kumar, Rakesh
Sangwan, M S
Mehta, Naresh
Sangwan, Naresh K
Issue Date: Aug-2001
Publisher: NISCAIR-CSIR, India
Abstract: Base catalyzed condensation of 4-hydroxyacetophenone 1 with araldehydes 2-8 yields 3-ary l-1-(4-hydroxyphenyl)prop-2-en-1-ones 9-15. compounds 9-15 are alkylated with ethyl chloroacetate to furnish ethyl [4-(3-arylprop-2-enoyl)phenoxylacetates 16-22. The esters 16-22 are subjected to nucleophilic displacement reactions with isopropylamine and morpholine to give the title compounds. 2-[4(-3-arylprop-2-noyl)phenoxy]-isopropyl acetamides 23-29 and 4-[{4-(3-arylprop-2-enoyl)phenoxy)acetyl]morpholine 30-36, respectively. The esters 16-22 are cyclized with excess of hydrazine hydrate in ethanol to give the title compounds, 2-[4-(5-aryl-4,5-dihydro-1H-pyrazol-3-yl)phenoxy]acetic acid hydrazides 37-43. All the compounds are tested for their toxicity against five phytopathogenic fungi. Rhizoctonia solani, Rhizoctonia bataticola, Sclerotinia sclerotiorum. Alternaria brassicae, and Fusarium solani, two saprophytic fungi Penicillium digitatum, and Aspergillus niger and one phytopathogenic bacterium Xanthomonas campestris pv. citrii. Some of the compounds inhibit the growth of S. sclerotiorum, A. niger and X. campestris pv. citrii at a concentration of 200 ppm.
Page(s): 682-687
URI: http://hdl.handle.net/123456789/22370
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.40B(08) [August 2001]

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