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Oxadiazolones, synthesis

In contrast to (74), compounds (75) are easily hydrolyzed to amidoximes. IV(4)-Alkylation of oxadiazolones (74) by oxiranes has been used for a synthesis of oxadiazines <75CBi9ll>. [Pg.196]

Synthesis, Insecticidal Activity, and Anticholinesterase Activity of Some Oxadiazolones... [Pg.241]

This report summarizes the synthesis, insecticidal activity, and anticholinesterase activity of some novel N-dihydrobenzo-furanyl oxadiazolones. The compounds were primarily aphicides with reduced activity on houseflies, corn earworms and two-spotted spider mites. Some of these gompounds were potent anticholineterases (I-. values 1-10x10 M) that were slowly reversible. There was little relationship between in vitro... [Pg.241]

The synthesis of these molecules can be broken down Into two parts. The first segment consisted of preparation of the dihydrobenzo-furanylhydrazines from which the oxadiazolones were eventually prepared. These hydrazines were prepared as follows the ap-... [Pg.242]

This report briefly summarizes the synthesis, insect toxicity and anticholinesterase activity of some novel dihydrobenzofuranyl oxadiazolones, a class of insecticides whose major strength lies in their toxicity to aphids with reduced activity on houseflies, two-spotted spider mites and corn earworms. This is similar to the previously reported RP 32,861, which also was most active on sucking insects. The molecule with the broadest toxicity spectrum... [Pg.247]


See other pages where Oxadiazolones, synthesis is mentioned: [Pg.187]    [Pg.243]    [Pg.245]    [Pg.247]    [Pg.249]    [Pg.129]    [Pg.194]   
See also in sourсe #XX -- [ Pg.617 , Pg.618 ]

See also in sourсe #XX -- [ Pg.617 , Pg.618 ]




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Oxadiazolones

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