Fmc Corporation

Bayer Cropscience Ag

Other

Stephen F Donovan

George Theodoridis

John W Lyga

Ping Ding

Walter H Yeager

Daniel H Cohen

Y Larry Zhang

Zeinab M Elshenawy

Robert N Henrie, Ii

David M Roush

Edward J Barron

John A Dixson

David Rosen

Thomas G Cullen

Ariamala Gopalsamy

Inna Shulman

Ian R Silverman

Paul E Rensner

Guozhi Wang

Seong Jae Yu

Qun Zhang

Dennis L Warkentin

Harvey Wendt

Benjamin J Dugan

Frank Zawacki

Dominic P Suarez

Saroj Sehgel

Manorama M Patel

Steven Shunxiang Zhang

Robert H Henrie, Ii

Olga Malsam

Roland Andree

Hans-Georg Schwarz

Christian Arnold

Eva-Maria Franken

Syed Z Ahmed

Shunxiang Zhang

Hongbin Men

Stephen Shunxiang Zhang

Certain substituted benzylamino heterocyclic and heteroaryl derivatives have provided unexpected insecticidal and acaricidal activity. These compounds are represented by formula (I): wherein R, R1, R2, R3, and R4 are fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula (I), and optionally, an effective amount of at least one of an additional compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present. 

Insecticidal substituted benzylamino heterocyclic and heteroaryl derivatives

Certain substituted amino heterocyclic and heteroaryl derivatives have provided unexpected insecticidal and acaricidal activity. These compounds are represented by formula (I): wherein R, R, R, R, R, A, B and Q are fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula I, and optionally, an effective amount of at least one of an additional compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present. 

Insecticidal substituted amino heterocyclic and heteroaryl derivatives

N-substituted azacycle derivative compounds represented by formula (I): 

N-substituted azacycles

It has now been found that certain novel heterocyclic derivitives have provided unexpected insecticidal activity. These compounds are represented by formula (I): R Preferred are those compounds of formula (I) where Rand R3 taken together is &#x2550;NCH(R)CH(R)N(R)&#x2014;, &#x2550;NC(R6)&#x2550;C(R7)N(R8)&#x2014;, or &#x2550;CHN&#x2550;C(R)N(R)&#x2014;, and tautomers thereof, and where Rand Rtaken together is &#x2014;C(R11)&#x2550;C(R12)C(R13)&#x2550;C(R14) 1 12, -, where R,R,R6, R7, R8, RI1, R R13, R14, and X are described. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula (I), and optionally, an effective amount of at least one of a second compound with at least one insecticidally compatable carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present. 

Pesticidal heterocycles

It has now been found that certain novel N-(substituted aryl)-4-(disubstituted methyl)piperidine and pyridine derivatives have provided unexpected insecticidal activity. These compounds are represented by formula (I): wherein m, n, q, r, and s are independently selected from 0 or 1; and p is 0, 1, 2, or 3; A is C or CH; and B, D, E, R, R, R, R, R, R, R, Rand Rare fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula I, and optionally, an effective amount of at least one of a second compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present.

N-(substituted arylmethyl)-4-(disubstituted methyl) piperidines and pyridines

Insecticidal (dihalopropenyl) phenylalkyl substituted dihydrobenzofuran and dihydrobenzopyran derivatives of Formula I are disclosed. These compounds provide unexpected insecticidal activity across a spectrum of insect pests combined with desirable physical properties including improved photostability. wherein x and y are integers independently selected from 0 or 1; and B is a bridging group*&#x2014;(CRR)&#x2014;(CRR)&#x2014;(CRR)-L-(CRR)&#x2014;(CRR)&#x2014;(CRR)&#x2014;,where the asterisk denotes attachment at A; and q, r, s, u, v and w are integers independently selected from 0, 1 and 2; and t is an integer selected from 0 and 1. A, D, E, G, M, R through R, and Rthrough R, inclusively, are fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula I and methods of controlling insects by applying said compositions to a locus where insects are present or are expected to be present are also disclosed.

Insecticidal (dihalopropenyl) phenylalkyl substituted dihydrobenzofuran and dihydrobenzopyran derivatives

A system dries water droplets within a person's outer and inner ear. The presence of the droplets is typically caused by swimming, showering, bathing, and other activities associated with water sports such as diving, water polo and the like. A hair dryer blows warm air at a distance into a handheld drying apparatus. One or more diffusion chambers containing a plurality of apertures deliver warm air from the hair dryer into the outer ear. An integral central tubular element forming part of the diffusion chamber delivers warm air from the hair dryer into the inner canal. The diffusion chamber has a handle to help position the central tubular element within the inner ear canal. The distance between the hair dryer and the handheld drying apparatus may be varied to select a comfortable warmth level and warm air velocity.

Outer and inner ear drying system

It has now been found that certain novel heterocyclic derivatives have provided unexpected insecticidal activity. These compounds are represented by formula (I): R Preferred are those compounds of formula (I) where Rand R3 taken together is &#x2550;NCH(R)CH(R)N(R)&#x2014;, &#x2550;NC(R6)&#x2550;C(R7)N(R8)&#x2014;, or &#x2550;CHN&#x2550;C(R)N(R)&#x2014;, and tautomers thereof, and where Rand Rtaken together is &#x2014;C(R11)&#x2550;C(R12)C(R13)&#x2550;C(R14) 1 12, &#x2014;, where R,R,R 6, R 7, R8, R I1, R R 13, R 14, and X are described. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula (I), and optionally, an effective amount of at least one of a second compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present 

It has now been found that certain novel N-(substituted aryl)-4-(disubstituted methyl)piperidine and pyridine derivatives have provided unexpected insecticidal activity. These compounds are represented by formula (I): wherein m, n, q, r, and s are independently selected from 0 or 1; and p is 0, 1, 2, or 3; A is CH or N; and B, D, E, R, R, R, R, R, R, R, Rand Rare fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula I, and optionally, an effective amount of at least one of a second compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present.

N-(substituted arylmethyl)-4-(disubstituted methyl)piperidines and piperazines

It has now been found that certain novel N-(substituted aryl)-4(disubstituted methyl)piperidine and pyridine derivatives have provided unexpected insecticidal activity. These compounds are represented by formula (I): wherein m, n, q, r, and s are independently selected from 0 or 1; and p is 0, 1, 2, or 3; A is C or CH; and B, D, E, R, R, R, R, R, R, R, Rand Rare fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula I, and optionally, an effective amount of at least one of a second compound, with at least one insecticidally compatible carrier are also disclosed; along with methods of controlling insects comprising applying said compositions to a locus where insects are present or are expected to be present 

Insecticidal (dihalopropenyl) phenylalkyl substituted dihydrobenzofuran and dihydrobenzopyran derivatives of Formula I are disclosed. These compounds provide unexpected insecticidal activity across a spectrum of insect pests combined with desirable physical properties including improved photostability.wherein x and y are integers independently selected from 0 or 1; and B is a bridging group*&#x2014;(CRR)&#x2014;(CRR)&#x2014;(CRR)&#x2014;L&#x2014;(CRR)&#x2014;(CRR)&#x2014;(CRR)&#x2014;,where the asterisk denotes attachment at A; and q, r, s, u, v and w are integers independently selected from 0, 1 and 2; and t is an integer selected from 0 and 1. A, D, E, G, M, R through R, and Rthrough R, inclusively, are fully described herein. In addition, compositions comprising an insecticidally effective amount of at least one compound of formula I and methods of controlling insects by applying said compositions to a locus where insects are present or are expected to be present are also disclosed.

Growing community of inventors

Revere, PA, United States of America

Stephen F Donovan