Dow Agrosciences LLC

Joe Raymond Schoonover

James Michael Gifford

Vidyadhar Babu Hegde

James Edwin Dripps

Katherine Anne Guenthenspberger

Laura Lee Karr

Scott Jerome Bis

Leonard P Dintenfass

Maurice Chee Hoong Yap

Denise Marie Perreault

Francis Eugene Tisdell

Timothy P Martin

Gary D Crouse

Thomas Clarence Sparks

Carl Vincent DeAmicis

Herbert A Kirst

Lawrence C Creemer

Peter Biagio Anzeveno

Michael John Ricks

Frederick Richard Green, Iii

Brian R Thoreen

Thomas V Worden

Christopher J Hatton

Kevin L McLaren

Jacek G Martynow

Triazole compounds having a 2,6-disubstituted-phenyl group in the 3-position, 5'-arylthien-2-yl group in the 5-position and an alkyl group in the 1-position are effective in controlling lepidoptera, coleoptera, mites and other sucking pests.

Insecticidal 3-(2,6-disubstituted phenyl)-5-[5-arylthien-2-yl]-1,2,4-triazoles

Triazole compounds having a 2,6-disubstituted-phenyl group in the 3-position, 5'-arylthien-3-yl group in the 5-position and an alkyl group in the 1-position are effective in controlling lepidoptera, coleoptera, mites and other sucking pests.

Insecticidal 3-(2,6-disubstituted phenyl)-5-[5-arylthien-3-yl]-1,2,4-triazoles

Oxazoline compounds having a 3,5-disubstituted-4-pyridyl group in the 2-position and a thienyl, thiazolyl or an arylphenyl group in the 4-position are effective in controlling aphids, insects and mites.

2-(3,5-Disubstituted-4-pyridyl)-4-(thienyl, thiazolyl or arylphenyl)-1,3-oxazoline compounds

Triazole compounds having a 2,6-disubstituted-phenyl group in the 3-position, arylthien-2- or -3-yl in the 5-position and an alkyl group in the 1-position are effective in controlling lepidoptera, coleoptera, mites and other sucking pests.

Insecticial 3-(2,6-disubstituted phenyl)-5-&lsqb;4- or 5-arylthien-2- or -3-yl&rsqb;-1,2,4-triazoles

Oxazoline compounds having a 2,6-disubstituted-phenyl group in the 2-position, an aryl or heteroaryl group in the 4-position and an alkyl group in the 5-position are effective in controlling aphids, insects and mites.

2-(2,6-disubstituted phenyl)-4-aryl-5-alkyl-1,3-oxazoline compounds

The compounds of the present invention are prepared directly or indirectly by modifying the compounds that are naturally produced from Saccharopolyspora spinosa. The compounds of the invention have been shown to have activity against insects and mites. The compounds are prepared by modifying the rhamnose sugar, modification of the forosamine sugar, or starting with pseuodoaglycone and then replacement with a nonsugar derivative or different sugar, modification of the 5,6,5-tricyclic and 12-membered macrocyclic lactone part of the compounds naturally produced or of the pseudoaglycone of the natural compounds.

Synthetic modification of Spinosyn compounds

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Joe Raymond Schoonover