137386-82-4Relevant academic research and scientific papers
Pesticidal cyclopropyl-2,4-dieneamides
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, (2008/06/13)
The present Application discloses pesticidally active compounds of the formula (I): or a salt thereof, wherein Q is an monocyclic aromatic ring. or fused bicyclic ring system of which at least one ring is aromatic containing 9 or 10 atoms of which one may be nitrogen and the rest carbon each optionally substituted, or Q is a dihalovinyl group or a group R6 --C C-- where R6 is C1-4 alkyl, tri C1-4 alkylsilyl, halogen or hydrogen; Q1 is a 1,2-cyclopropyl ring optionally substituted by one or more groups selected from C1-3 alkyl. halo, C1-3 haloalkyl, alkynyl, or cyano; R2,R3, R4 and R5 are the same or different with at least one being hydrogen and the others being independently selected from hydrogen, halo. C1-4 alkyl or C1-4 haloalkyl; X is oxygen or sulphur; and R1 is selected from hydrogen and C1-8 hydrocarbyl optionally substituted by dioxalanyl, halo, cyano, trifluoromethyl, trifluoromethylthio or C1-6 alkoxy. their preparation, pesticidal compositions containing them and their use against pests.
Cyclopropyl derivative lipoxygenase inhibitors
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, (2008/06/13)
Certain carbocyclic aryl- and heterocyclic aryl- substituted cyclopropyl N-hydroxyureas, N-hydroxy-carboxamides, and N-acyl-N-hydroxyamines inhibit 5- and/or 12-lipoxygenase and are useful in the treatment of inflammatory disease states.
CYCLOPROPYL DERIVATIVE LIPOXYGENASE INHIBITORS
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, (2008/06/13)
Certain carbocyclic aryl- and heterocyclic aryl-substituted cyclopropyl N-hydroxyureas, N-hydoroxycarboxamides, and N-acyl-N-hydroxyamides inhibit 5- and/or 12-lipoxygenase and are useful in the treatment of inflammatory disease states
RING OPENING REACTION OF gem-DIFLUOROCYCLOPROPYL KETONES WITH NUCLEOPHILES
Kobayashi, Yoshiro,Taguchi, Takeo,Morikawa, Tsutomu,Takase, Toyohiko,Takanashi, Hiroshi
, p. 1047 - 1050 (2007/10/02)
Syntheses of gem-difluorocyclopropyl ketones (3a-d) and their reactions with nucleophiles are described.Ring opening reactions of 3a, c and d with a methanolate and a thiolate anion took entirely different courses of bond scission of the cyclopropane ring.
