IP Library › Granted Patent US 9,198,419
Granted Patent B2
US 9,198,419 · App. 13/887,998 · Granted Dec 1, 2015

Use of pro-fungicides of UK-2A for control of black sigatoka

Inventors: W. John Owen (Carmel, IN); Leonardo Paniagua (Madrid, ES); David G. Oimette (Carmel, IN)
Assignee: Dow AgroSciences LLC
A01N43/40C07D405/12
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Quick Facts
Patent No.
US 9,198,419
App. No.
13/887,998
Granted
Dec 1, 2015
Kind
B2
Abstract

The present disclosure is related to the field of agrochemicals, including profungicides of UK-2A and their use to control Black Sigatoka.

Claims (30)

1. A method of treating a plant, comprising the steps of:

contacting at least one portion of a plant with a composition including a compound of Formula I:

wherein M is selected from —R1, —C(O)R1, —C(O)OR1, —C(S)OR1, —C(O)N(R1)R2, —CH2C(O)R1, —CH2OC(O)R1, —CH2C(S)OR1, —CH2C(O)N(R1)R2 —CH2OR1, —CH2SR1, —CH2P(O)2OR1, —Si(R1)3, —S(O)2OR1, P(O)2OR1;

R1 is alkyl or arylalkyl; and

R2 is alkyl or arylalkyl,

wherein the plant has been or is at risk for being exposed to a plant pathogen, and wherein the plant pathogen is Mycosphaerella fijiensis ; and

wherein the compound of Formula I is present in the composition at a concentration of about 50 to about 1000 ppm.

2. A method of treating a plant, comprising the steps of:

contacting an area adjacent to a plant with a composition including a compound of Formula I:

wherein M is selected from —R1, —C(O)R1, —C(O)OR1, —C(S)OR1, —C(O)N(R1)R2, —CH2C(O)R1, —CH2OC(O)R1, —CH2C(S)OR1, —CH2C(O)N(R1)R2 —CH2OR1, —CH2SR1, —CH2P(O)2OR1, —Si(R1)3, —S(O)2OR1, P(O)2OR1;

R 1 is alkyl or arylalkyl; and

R 2 is alkyl or arylalkyl,

wherein the plant has been or is at risk for being exposed to a plant pathogen, and wherein the pathogen is Mycosphaerella fijiensis ; and

wherein the compound of Formula I is present in the composition at a concentration of about 50 to about 1000 ppm.

3. The method of claim 1 , wherein the compound of Formula I is:

4. The method of claim 1 , wherein the composition further includes at least one additional agriculturally active ingredient selected from the group consisting of: an insecticide, an herbicide, and a fungicide.

5. The method of claim 1 , wherein the concentration is about 50 to about 500 ppm.

6. The method of claim 5 , wherein the concentration is about 50 to about 300 ppm.

7. The method of claim 1 , wherein the compound is applied to the plant at an application rate of 50 to 400 g/Ha.

8. The method of claim 1 , wherein the plant comprises a banana plant.

9. The method of claim 2 , wherein the compound of Formula I is:

10. The method of claim 2 , wherein the composition further includes at least one additional agriculturally active ingredient selected from the group consisting of: an insecticide, an herbicide, and a fungicide.

11. The method of claim 2 , wherein the concentration is about 50 to about 500 ppm.

12. The method of claim 11 , wherein the concentration is about 50 to about 300 ppm.

13. The method of claim 2 , wherein the compound is applied to the area adjacent the plant at an application rate of 50 to 400 g/Ha.

14. The method of claim 2 , wherein the plant comprises a banana plant.

15. The method of claim 3 , wherein the concentration is about 50 to about 500 ppm.

16. The method of claim 15 , wherein the concentration is about 50 to about 300 ppm.

17. The method of claim 9 , wherein the concentration is about 50 to about 500 ppm.

18. The method of claim 17 , wherein the concentration is about 50 to about 300 ppm.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 5, 2015
From: OWEN, W. JOHN; OUIMETTE, DAVID G; PANIAGUA, LEONARDO
To: DOW AGROSCIENCES LLC
Reel/Frame 036262/0709 →
Continuity (2)
Provisional Application 61643630 · May 7, 2012
Related Publication 20130296374A1 · Nov 7, 2013