Eli Lilly and Company

Dowelanco

Other

Barry A Dreikorn

Robert G Suhr

Glen P Jourdan

Kenneth E Kramer

Thomas D Thibault

Michael J Coghlan

James D Davenport

A Frederick Elsasser

Eriks V Krumkalns

Neil Vincent Kirby

Ronald E Hackler

Ronnie G Edie

Brian R Thoreen

Leon N Davis

Sylvester V Kaster

Blake A Caley

Substituted quinazolines of the formula (1): ##STR1## wherein: R.sup.1 to R.sup.4 are independently H, halo, (C.sub.1 -C.sub.4) alkyl, branched (C.sub.3 -C.sub.4) alkyl, halo (C.sub.1 -C.sub.4) alkyl, (C.sub.1 -C.sub.4) alkoxy, NO.sub.2, or NH.sub.2,

Quinazoline derivatives

Compounds of the formula (I): ##STR1## wherein: Het is pyridyl, pyrazinyl, pyrimidinyl, or pyridizinyl, optionally substituted with one or more groups selected from halo, lower alkyl, lower alkoxy, haloalkyl, haloalkoxy, NO.sub.2, CN, and lower alkoxy-carbonyl;

4-(2-(4-(2-pyridinyloxy)phenyl)ethoxy)quinazoline and analogues thereof

The compounds of the formula: ##STR1## wherein the substituents are herein below defined; are plant fungicides, insecticides, and miticides.

Quinoline derivatives

The compounds of the formula: ##STR1## where the substituents are herein below defined, are fungicides, insecticides, and miticides.

Substituted quinolines and cinnolines

Substituted naphthyridines of the formula (1): ##STR1## wherein one of A, B, C, or D is N, and the others are CR.sup.1 ;

Naphthyridine derivatives

A method of inhibiting a nematode population which comprises applying to the locus of a nematode, a nematode inactivating amount of a compound of the formula (1):

Quinoline nematicidal method

A fungicidal method which comprises applying to the locus of a plant pathogen a fungicidally effective but non-phytotoxic amount of a compound of the formula (1) ##STR1## wherein: R.sup.1 to R.sup.4 are independently

Substituted quinolines and cinnolines as fungicides

Novel alkyl-dinitrodiphenylamine compounds are useful in controlling insects and arachnids. These compounds are useful especially in the control of citrus rust mite.

Diphenylamine compounds

The present invention is directed to the use of a class of N-alkyldiphenylamines as insecticides and arachnicides, and also as ectoparasiticides. The invention is also directed to a class of novel fluorinated N-alkyldiphenylamines.

A class of 2,4,6-trinitrodiphenylamines, bearing one or more substituents on the ring which does not bear nitro groups, which substituents are chosen from among trfluoromethyl groups, nitro groups, and other simple substituents, are effective in the control of foliar phytopathogens.

2,4,6-Trinitrodiphenylamines for control of foliar phytopathogens

A class of isoxazoles having a phenyl or substituted-phenyl group at the 3-position and a substituted-methyl group at the 5-position are useful for the control of fungal foliar phytopathogens.

Fungicidal 3-phenyl-5-(substituted methyl)isoxazoles

A series of new diphenylamines have small alkyl substituents on the amino nitrogen. One phenyl ring bears dinitro-trifluoromethyl substitution, and the other is preferably substituted with halogen or pseudo-halogen groups. The new diphenylamines are useful as rodenticides.

Rodenticidal N-alkyldiphenylamines

A new class of substituted 2,6-dinitrobenzenamines bearing a chlorine atom in the 3-position, active against a number of plant pathogenic fungi, as well as methods for the use of the compounds and fungicidal compositions containing the compounds.

3-Chloro-2,6-dinitro-N-(substituted

Certain substituted N-pyridyl-N-phenylamines as rodenticides.

Growing community of inventors

Indianapolis, IN, United States of America

Barry A Dreikorn