Dow Agrosciences LLC

University of Notre Dame Du Lac

Other

George E Davis

Marvin J Miller

Garrett C Moraski

Lowell D Markley

Beth Lorsbach

David Hamilton Young

W John Owen

Kristy Bryan

Francis Eugene Tisdell

Maurice C H Yap

Chenglin Yao

James M Renga

Kevin Gerald Meyer

Timothy P Martin

William C Lo

Richard Brewer Rogers

Jeffrey Brian Epp

Michael Thomas Sullenberger

Bassam S Nader

Jeffery Dale Webster

Zoltan Laszlo Benko

Maurice C Yap

Mark Andrew Pobanz

Gary David Gustafson

Timothy A Boebel

James M Ruiz

Matthew J Henry

Paul Richard Graupner

Clive Waldron

Nneka Tuere Breaux

Gina Marie Fitzpatrick

Frisby Davis Smith

Todd L Werk

Ann B Orth

Amy J Smith

Shelvie J Davis

Francis Tisdell, Jr

Nneka Breaux

James Ruiz

David Young

Embodiments relate to the field of chemistry and biochemistry, and, more specifically, to imidazopyridine compounds, synthesis thereof, and methods of using same. Disclosed herein are various imidazo[1,2-a]pyhdine compounds and methods of using the novel compounds to treat or prevent tuberculosis in a subject or to inhibit fungal growth on plant species. Other embodiments include methods of synthesizing imidazo[1,2-a]pyridine compounds, such as the disclosed imidazo[1,2-a]pyridine compounds.

Imidazo [1,2-a]pyridine compounds, synthesis thereof, and methods of using same

This present disclosure is related to the field of 5-fluoro pyrimidines and their derivatives and to the use of these compounds as fungicides.

5-fluoro pyrimidine derivatives

This present disclosure is related to the field of pyrazine carboxamides and their derivatives and the use of these compounds as fungicides.

Pyrazinyl carboxamides as fungicides

Various aspects disclosed herein relate to aryl substituted aminopyrimidines according to Formula 1: wherein, Xis N or C&#x2014;R; Xis N or C&#x2014;Rprovided that Xand Xare not both N; R-Rare H, CN, CHO, &#x2014;SCN, NO, F, Cl, Br, I, substituted or unsubstituted C1-C4-alkyl, substituted or unsubstituted halo-C1-C4-alkyl, substituted or unsubstituted C1-C4-alkoxy, substituted or unsubstituted halo-C1-C4-alkoxy, substituted or unsubstituted C1-C4-thioalkyl, substituted or unsubstituted halo-C1-C4-thioalkyl, substituted or unsubstituted C3-C-7-cycloalkyl, substituted or unsubstituted C2-C4-alkenyl, C2-C4-alkynyl, substituted or unsubstituted C1-C4-acylalkyl, C1-C4-acyloxy, C1-C4 alkoxycarbonyl, C1-C4-alkoxy-amino, C1-C4-alkyl-S(O)&#x2550;NH, substituted or unsubstituted aryl, substituted or unsubstituted heterocycle, wherein the substituents are one or more of the following F, Cl, Br, OH, CN, NO, CHO, &#x2014;SCN, S(O)n-C1-C4-alkyl (where n=0-2), C1-C4-alkyl, halo-C1-C4-alkyl, C1-C4-alkylamine, C1-C4-alkoxy, halo-C1-C4-alkoxy, C1-C4-thioalkyl, halo-C1-C4-thioalkyl, C1-C4-alkylacyl, C1-C4-acyloxy, C1-C4 alkoxycarbonyl, C1-C4-alkoxy-imino, hydroxy-imino; C1-C4-alkyl-S(O)&#x2550;NH; and Q is a substituted or unsubstituted aryl, substituted or unsubstituted heterocycle wherein the substituents of Q are taken from R-R.

Compounds and methods for controlling fungi

Fungicidal compositions and methods comprising acylated aminosalicylamides (AASA) described herein. Novel amines and 3-nitrosalicylamides, and their use as pesticides and in the preparation of the antifungal AASA compounds are also disclosed.

Fungicidal compositions and methods, and compounds and methods for the preparation thereof

Dihydroorotate dehydrogenase (DHOD) inhibititon assays are utilized in a method for identifying new fungicides; DHOD inhibitors are useful in fungicidal methods and compositions. Resistance genes that are mutants of the wild-type Aspergillus nidulans dihydroorotate dehydrogenase gene have been isolated and found to impart resistance to certain DHOD inhibitors. The resistance genes are useful as selectable markers in fungi. The wild-type gene is also provided.

Method of identifying potential fungicides using dihydroorotate

A releasably mounted back rest is provided including a cushion and a pair of vertical stanchions coupled at top ends thereof to the rear surface of the cushion extended downwardly a predetermined distance. Also included is a joint assembly comprising a pair of lower members hingably coupled to the stanchions. By this structure, the stanchions and lower members of the joint assembly are adapted to pivot between a first orientation wherein the same are linearly aligned and a second orientation wherein the same are situated perpendicular with respect to each other. Lastly, a clamp is situated at bottom ends of the lower members for releasably coupling with a seat.

Back rest

Growing community of inventors

Carmel, IN, United States of America

George E Davis