Dow Agrosciences LLC

Corteva Agriscience LLC

Other

Noormohamed Mohamed Niyaz

Ricky Hunter

Tony K Trullinger

Yu Zhang

Ann Marie Buysse

Negar Garizi

Ronald Ross, Jr

Daniel Knueppel

Carl Vincent DeAmicis

Christian Thomas Lowe

Timothy Calvin Johnson

David Anthony Demeter

Asako Kubota

Martin J Walsh

Annette Vitale Brown

Dan Pernich

Kevin Gerald Meyer

William Hunter Dent, Iii

Gary A Roth

Richard Brewer Rogers

Kristy Bryan

CaSandra Lee McLeod

Paul Renee LePlae, Jr

Maurice C H Yap

Chenglin Yao

Yuanming Zhu

Akshay Patny

Bassam S Nader

Beth Lorsbach

Jeffrey S Nissen

Qiang Yang

Kaitlyn C Gray

Robert Peter Gajewski

John L Miesel

Irene Mae Morrison

Michael John Ricks

Gina Marie Fitzpatrick

Gregory T Whiteker

Gary D Crouse

James M Renga

Thomas Clarence Sparks

Joseph D Eckelbarger

Peter Lee Johnson

Katherine Anne Guenthenspberger

Frank J Wessels

Greg Whiteker

Marshall H Parker

Carl DeAMICIS

Paul R LePlae

Carl Deamicis

Kim Eric Arndt

Jeremy Kister

Peter S Borromeo

Emily Marie Rigsbee

William Thomas Lambert

Ronald Ross

William C Lo

Gerald Bryan Watson

Natalie Christine Giampietro

Lindsey Gayle Fischer

Erich W Baum

Chunming Zhang

Francis Eugene Tisdell

Ronald B Leng

Matthew J Henry

Rong Ling

Nicholas Martin Irvine

Jaime Susanne Nugent

Scott P West

Thomas J Barton

Abraham D Schuitman

Siyu Tu

Jayachandran Devaraj

Jenifer L Adamski Butz

Melissa Lee

Aaron A Shinkle

Nugzar Ghavtadze

Casandra L Mcleod

Paul R Schmitzer

Norbert M Satchivi

Thomas L Siddall

Steven H Shaber

Jeffrey Brian Epp

Michael Thomas Sullenberger

Maurice C Yap

Brent Jeffrey Rieder

Peter Biagio Anzeveno

Jeff Petkus

Nick X Wang

William Randal Erickson

Maurice Chee Hoong Yap

Lindsey G Horty

Frisby Davis Smith

Jenifer Lynn Adamski Butz

Rongrong [mandy] Lin

Rongrong (Mandy) Lin

William Hunter Dent

William Dent

Bassam Salim Nader

Jennifer Lynn Adamski Butz

Methods for preparing 5-fluoro-6-(bromo or chloro)picloram analogs, or derivatives thereof, from picloram acid, picloram ester, or the nitrile analog of picloram are provided. The methods include chemical process steps that: (1) introduce a phthaloyl group onto the 4-amino substituent of picloram acid, picloram ester, or the nitrile analog of picloram, (2) add 2 fluorine atoms at the 5,6-positions of the pyridine ring using halex fluorination chemistry, (3) remove the phthaloyl group, hydrolyze the ester or nitrile substituent, and add chlorine or bromine to the 6-position by treatment with an acid and water, and finally, (4) esterify the 5-fluoro-6-(bromo or chloro)picloram acid produced in step (3) to a 5-fluoro-6-(bromo or chloro)picloram ester.

Preparation of halogen analogs of picloram

Described herein are 4-amino-6-(1,3-benzodioxole)picolinic acids, compositions comprising 4-amino-6-(1,3-benzodioxole)picolinic acids, and the use of these compounds and compositions to control undesirable vegetation.

4-amino-6-(1,3-benzodioxole)picolinates and their use as herbicides

A pesticidal composition comprises a compound of formula I or any agriculturally acceptable salt thereof, wherein R, R, R, R, R, R, Z, Q, and Y are as described herein. A method of controlling pests comprises applying the pesticidal composition near a population of pests, or to an area to control pests.

Pesticidal compositions and related methods

This document discloses molecules having the following formula ('Formula One'): and processes related thereto.

Pesticidal compositions and processes related thereto

The present application provides processes for making pesticidal compounds and compounds useful both as pesticides and in the making of pesticidal compounds.

Processes for the preparation of pesticidal compounds

A pesticidal composition comprises at least one compound selected from a 1-(3-pyridyl-N-oxide) pyrazole compound of formula I, II, or III, or any agriculturally acceptable salt thereof, wherein R, R, R, R, R, R, R, R, R, R, Y, and Q, are as described herein. A method of controlling pests comprises applying the pesticidal composition near a population of pests. 

A process of applying a pesticidal composition to an area to control a pest, wherein the pesticidal composition comprises at least one compound selected from a compound of formula I, or any agriculturally acceptable salt thereof, wherein R, R, R, R, R, R, R, R, Q, Z, L, L, and x are as described herein. A method of controlling pests comprises applying the pesticidal composition near a population of pests. 

A pesticidal composition comprises a 3-(1H-pyrazol)pyridine compound of formula I or any agriculturally acceptable salt thereof, wherein R, R, R, R, R, R, R, R, R, R, x, n, and Q are as described herein. A method of controlling pests comprises applying the pesticidal composition near a population of pests. 

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the following formula ('Formula One'). 

Molecules having certain pesticidal utilities, intermediates, compositions, and processes, related thereto

A pesticidal composition comprises one or more of the following compounds: 3-(thiazol-2-yl)pyridine 1-oxide compound of formula I or II, or N-(4-chloro-2-(pyridin-3-yl)thiazol-5-yl)-3-(methylthio)propanamide compound (C3), or any agriculturally acceptable salt thereof, wherein R, R, R, R, R, R, R, and Q, are as described herein. A method of controlling pests comprises applying the pesticidal composition near a population of pests. 

Growing community of inventors

Indianapolis, IN, United States of America

Noormohamed Mohamed Niyaz