Dow Agrosciences LLC

University of Illinois

Corteva Agriscience LLC

Dow Global Technolgoies LLC

Kaitlyn C Gray

Qiang Yang

Beth Lorsbach

Yu Zhang

Carl Vincent DeAmicis

Gary A Roth

Ronald Ross, Jr

Joseck M Muhuhi

Gregory T Whiteker

Greg Whiteker

Jeffrey S Nissen

Timothy P Martin

Joseph D Eckelbarger

Thomas P Clark

Daniel Knueppel

John F Daeuble, Sr

Ronald J Heemstra

Gary D Crouse

Nakyen Choy

Maurice C Yap

Erich W Baum

Stephen Scott Davis

David D Devore

Stephen J Davis

Ricky Hunter

Tony K Trullinger

David Anthony Demeter

Zoltan Laszlo Benko

Fangzheng Li

Frank J Wessels

Michelle Bowerman Riener

Peter Vednor

Belgin Canturk

Elisabeth J Kane

Thomas Clarence Sparks

Noormohamed Mohamed Niyaz

Martin D Burke

Monica Britt Olson

David M Knapp

Ian Dailey

Justin Robert Struble

Brice E Uno

Pulin Wang

Nagarjuna Palyam

Ann Marie Buysse

David E Podhorez

Xiaoyong Li

Kyle A Dekorver

Kyle A DeKorver

Nicolaas Vermeulen

Alex Nolan

Nicholas R Babij

Yan Hao

Jeff Nissen

Shaoguang Feng

Sukrit Mukhopadhyay

Eric P Gillis

David Laitar

David M Pearson

Liam P Spencer

Jing Yan

Robert Froese

Robert J Wright

John F Daeuble

Aaron A Rachford

Jichang Feng

Sarah Ryan

Tom Sparks

Justin Struble

Suk Joong Lee

Stephen Davis

Ronald Ross

Kyla A Dekorver

Zoltan L Venko

Jr Ronald Ross

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

Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto

Provided are certain derivatives of amphotericin B (AmB) characterized by reduced toxicity and retained anti-fungal activity. Certain of the derivatives are C16 urea derivatives of AmB. Certain of the derivatives are C3, C5, C8, C9, C11, C13, or C15 deoxy derivatives of AmB. Certain of the derivatives include C3′ or C4′ modifications of the mycosamine appendage of AmB. Also provided are methods of making AmB derivatives of the invention, pharmaceutical compositions comprising AmB derivatives of the invention, and methods of use of AmB derivatives of the invention.

Amphotericin B derivatives with improved therapeutic index

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

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

Provided are certain derivatives of amphotericin B (AmB) characterized by reduced toxicity and retained anti-fungal activity. Certain of the derivatives are C16 urea derivatives of AmB. Certain of the derivatives are C3, C5, C8, C9, C11, C13, or C15 deoxy derivatives of AmB. Certain of the derivatives include C3' or C4&#x2032; modifications of the mycosamine appendage of AmB. Also provided are methods of making AmB derivatives of the invention, pharmaceutical compositions comprising AmB derivatives of the invention, and methods of use of AmB derivatives of the invention.

Molecules having pesticidal utility, and intermediates, compositions, and processes related thereto

Provided herein is a process for the preparation of 4-((6-(2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy-3-(5-mercapto-1H-1,2,4-triazol-1-yl)propyl)pyridin-3-yl)oxy)benzonitrile.

4-((6-(2-(2,4-difluorophenyl)-1,1-difluoro-2-hydroxy-3-(5-mercapto-1h-1,2,4-triazol-1-yl)propyl)pyridin-3-yl)oxy)benzonitrile and processes of preparation

Provided herein is a process for the preparation of 4-((6-bromopyridin-3-yl)oxy)benzonitrile.

4-((6-bromopyridin-3-yl)oxy)benzonitrile and processes of preparation

The present disclosure provides a composition comprising at least one compound selected from the group consisting of Compound 1, Compound 2, and combinations thereof, as shown below, and described herein: wherein, for Compound 1 and Compound 2, independently, Rand Reach independently is selected from the group consisting of hydrogen, a substituted alkyl, an unsubstituted alkyl, a substituted heteroalkyl, an unsubstituted heteroalkyl, a substituted aryl, an unsubstituted aryl, a substituted heteroaryl and an unsubstituted heteroaryl; wherein, for Compound 1 and Compound 2, independently, the Component A is selected from the group consisting of Group a) through Group h): wherein Group a) through Group h) are described herein.

Fluorene derivatives as light emitting elements for electroluminescent devices

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

Molecules having pesticidal utility and intermediates, compositions and processes related thereto

Growing community of inventors

Freeland, MI, United States of America

Kaitlyn C Gray