Zobrazeno 1 - 10
of 30
pro vyhledávání: '"DAVID A. PULMAN"'
Autor:
David A. Pulman
Publikováno v:
Journal of Agricultural and Food Chemistry. 59:2770-2772
Replacement of the pyrethronyl alcohol portion of the natural pyrethrins with the 5-benzyl-3-furylmethyl moiety gave bioresmethrin, a synthetic pyrethroid of high potency and safety but with limited photostability. Introduction of novel substituents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e50b252dbb2262f5c5513a08e3b79f9d
https://doi.org/10.1021/jf102256s
https://doi.org/10.1021/jf102256s
Publikováno v:
Pesticide Science. 46:237-245
5-tert-Butyl-2-(4-ethynylphenyl)pyrimidine and the corresponding 2,5-disubstituted-4H-1,3-thiazine block the GABA-gated chloride channel at c.20 and c.200 nM, respectively, measured as 50% inhibition of the binding of 1-(4-ethynylphenyl)-4-[ 3 H]prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55ef18550679d321d5a0203561d25185
https://doi.org/10.1002/(sici)1096-9063(199603)46:3<237::aid-ps359>3.0.co
https://doi.org/10.1002/(sici)1096-9063(199603)46:3<237::aid-ps359>3.0.co
Publikováno v:
Pesticide Science. 44:69-74
4-tert-Butyl-2,6,7-trioxabicyclo[2.2.2]octanes and 5-tert-butyl- 1,3-dithianes with the 4-ethynylcyclohexyl substituent in the 1- and 2-positions, respectively, are potent insecticides modeled on their 4-ethynylphenyl and hex-5-ynyl analogs. The comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::835d129df76df40e0e0b595670335f8f
https://doi.org/10.1002/ps.2780440110
https://doi.org/10.1002/ps.2780440110
Publikováno v:
Journal of Agricultural and Food Chemistry. 40:147-151
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7130d3da07141cfa18f190c234a9bfa1
https://doi.org/10.1021/jf00013a029
https://doi.org/10.1021/jf00013a029
Publikováno v:
Pesticide Science. 18:223-228
Substituted phenylacetaldehydes, made by homologation of the benzaldehydes by Wittig condensation with a methoxymethylene ylid, were condensed under Wadsworth-Emmons conditions to give the substituted N-(2-methylpropyl)-6-phenylhexa-2,4-dienamides. E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a18944bf976bd4ac68cbbf6bf3ce7381
https://doi.org/10.1002/ps.2780180402
https://doi.org/10.1002/ps.2780180402
Publikováno v:
Pesticide Science. 18:191-201
A group of naturally occurring isobutylamides and related compounds exhibit a range of biological properties including activity against insects. Their potential as a starting point for developing new insecticides, needed to control pests resistant to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9506ba6a45db749e391823b784d8299a
https://doi.org/10.1002/ps.2780180305
https://doi.org/10.1002/ps.2780180305
Publikováno v:
Pesticide Science. 7:499-502
The insecticidal activities against houseflies (Musca domestica L.) and mustard beetles (Phaedon cochleariae Fab.) of 29 new 5-benzyl-3-furylmethyl 2,2-dimethyl-cyclopropane-carboxylates are compared with those of the corresponding chrysanthe-mate (b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::485139a60a25be4a54849c66f83547fd
https://doi.org/10.1002/ps.2780070512
https://doi.org/10.1002/ps.2780070512
Publikováno v:
Pesticide Science. 18:203-209
Following the discovery of insecticidal activity in (2E,4E)-N-(2-methylpropyl)-6-phenylhexa-2,4-dienamide, structural analogues containing variations of the central pentadiene system have been examined. They include the five compounds with extra meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::729d8930eb50839232bfcf615bb02dc1
https://doi.org/10.1002/ps.2780180306
https://doi.org/10.1002/ps.2780180306
Publikováno v:
Pesticide Science. 9:105-111
Preparation of 3-phenoxybenzyl chrysanthemates and their dihalovinyl analogues substituted with a cyano group at the 2-, 6-, (R)-α-, or (S)-α- positions is described. The (R)- and (S)- isomers of α-cyano-3-phenoxybenzyl esters of 2,2-difluoro-, -d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edff0af71806bf22bfbf81f3909aa13a
https://doi.org/10.1002/ps.2780090203
https://doi.org/10.1002/ps.2780090203
Autor:
Paul E. Burt, Norman F. Janes, Michael Elliott, David A. Pulman, P. H. Needham, Andrew W. Earnham
Publikováno v:
Pesticide Science. 5:791-799
Esters of 2,2-dimethyl-3-(2,2-dichlorovinyl)-cyclopropanecarboxylic acid with appropriate alcohols are more active insecticides than the corresponding 3-isobutenyl compounds (chrysanthemates). (±)-Cis and (±)-trans forms of the dichloro acid are ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82ac4bbd11ef05da4ced7d564e63f1a1
https://doi.org/10.1002/ps.2780050614
https://doi.org/10.1002/ps.2780050614