In:
Journal of Heterocyclic Chemistry, Wiley, Vol. 54, No. 2 ( 2017-03), p. 1121-1128
Abstract:
Using cyenopyrafen as the lead compound, a series of novel pyrazole acrylonitrile compounds were designed and synthesized via the reaction of butylphenylacetonitrile with the corresponding (substituted pyrazol‐5‐yl) methanone of pyrethroid alcohols in the presence of potassium tert‐butoxide. These compounds showed prominent acaricidal activity against Tetranchus urticae . In particular, IIf , IIh , IIo , and IIp displayed excellent activities, which the median lethal concentrations were all lower 0.4 mg/L. In addition, the structure‐activity relationship for the target compounds was discussed.
Type of Medium:
Online Resource
ISSN:
0022-152X
,
1943-5193
Language:
English
Publisher:
Wiley
Publication Date:
2017
detail.hit.zdb_id:
218131-9
detail.hit.zdb_id:
2042274-X
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