| Patent Number |
Title Of Patent |
Date Issued |
| RE39991 |
Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
January 1, 2008 |
| A compound having the following formula: ##STR00001## wherein R.sub.3 and M are defined herein, and processes therewith. |
| 7034035 |
Fungicidal mono-, bi-, and tri-cycloheteroalkyl amides and their compositions, methods of use an |
April 25, 2006 |
| The present invention relates to compounds of Formula I: ##STR00001## wherein: a) ##STR00002## represents a 6-membered heterocyclic aromatic ring in which X.sub.1 is N and X.sub.2, X.sub.3 and X.sub.4 are each independently CR''; R'' is independently H, halogen, cyano, hydroxy |
| 6927225 |
Fungicidal 2-pyridyl alkyl amides and their compositions, methods of use and preparation |
August 9, 2005 |
| The present invention relates to compounds of Formula I: ##STR1##wherein: ##STR2##represents a 6-membered heterocyclic aromatic ring in which X.sub.1 is N, and X.sub.2, X.sub.3 and X.sub.4 are CR"; wherein R" is independently H, halogen, cyano, hydroxy, C.sub.1 -C.sub.3 alkyl, C.s |
| 6706740 |
Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
March 16, 2004 |
| Heterocyclic aromatic amides (HAA) according to Formula I: ##STR1##wherein X.sub.1 -X.sub.4, M, Z, and A are herein defined. The invention also encompasses hydrates, salts and complexes thereof. These compounds are useful as antifungal agents. |
| 6521622 |
Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
February 18, 2003 |
| Heterocyclic aromatic amides having a hydroxy group adjacent to the amide functionality are useful as antifungal agents, particularly for plants. |
| 6355660 |
Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
March 12, 2002 |
| A compound having the following formula: ##STR1##wherein R.sub.3 and M are defined herein, and processes therewith. |
| 6297401 |
Fungicidal compositions and methods, and compounds and methods for the preparation thereof |
October 2, 2001 |
| Fungicidal compositions and methods comprising acylated aminosalicylamides (AASA) described herein. Novel cyclic amines and 3-nitrosalicylamides, and their use as pesticides and in the preparation of the antifungal AASA compounds are also disclosed. |
| 6001981 |
Synthetic modification of Spinosyn compounds |
December 14, 1999 |
| The compounds of the present invention are prepared directly or indirectly by modifying the compounds that are naturally produced from Saccharopolyspora spinosa. The compounds of the invention have been shown to have activity against insects and mites. The compounds are prepared by m |
| 5493024 |
3,4,N-trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insectioides |
February 20, 1996 |
| 3,4,N-triaryl-4,5-dihydro-1H-pyrazole-1-carboxamide compounds having an aryl moiety in the 4-position that is an optionally substituted pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or quinolinyl moiety and aryl moieties in the 3-position and the N-position that are optionally subs |
| 5418247 |
3,4,N-trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insecticides |
May 23, 1995 |
| 3,4,N-Trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamide compounds wherein the substituent in the 4-position is a 5-membered heterocyclic ring moiety containing one ring oxygen or sulfur atom and one or two ring nitrogen atoms and the substituents in the 3-posit ion and the N-position |
| 5338856 |
3,4-N,trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insecticides |
August 16, 1994 |
| 3,4,N-Trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamide compounds wherein the substituent in the 4-position is a 5-membered heterocyclic ring moiety containing one ring oxygen or sulfur atom and one or two ring nitrogen atoms and the substituents in the 3-position and the N-position |
| 5324837 |
3,4-disubstituted-4,5-dihydro-1H-pyrazoles and a method of preparation |
June 28, 1994 |
| 3,4-Diaryl-4,5-dihydro-1H-pyrazole compounds having a selected 5- or 6-membered aromatic heterocyclic moiety in the 4-position and an optionally substituted phenyl moiety in the 3-position, such as 4,5-dihydro-3-(4-fluorophenyl)-4-(5-trifluoromethyl-2-pyridinyl)-1H-pyrazo le were prep |
| 5250532 |
3,4,N-trisubstituted-4,5-dihydro-1H-pyrazole-1-carboxamides and their use as insecticides |
October 5, 1993 |
| 3,4,N-triaryl-4,5-dihydro-1H-pyrazole-1-carboxamide compounds having an aryl moiety in the 4-position that is an optionally substituted pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, or quinolinyl moiety and aryl moieties in the 3-position and the N-position that are optionally subs |
| 4419514 |
Method for converting carboxylic acid groups to trichloromethyl groups |
December 6, 1983 |
| Method for converting carboxylic acid groups to trichloromethyl groups which comprises contacting a compound containing a carboxylic acid group with a phenylphosphonic dichloride and phosphorus pentachloride and recovering the thus produced product. |
| 4281133 |
Substituted phenoxy and phenylthio picolinaldehydes |
July 28, 1981 |
| Substituted phenoxy and phenylthio picolinaldehydes are prepared which correspond to the formula: ##STR1## wherein X independently represents alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, alkylthio of 1 to 4 carbon atoms, alkylsulfonyl of 1 to 4 carbon atoms, trifl |
| 4256893 |
Substituted phenoxy and phenylthio pyridine methanols and substituted methanols |
March 17, 1981 |
| Substituted phenoxy and phenylthio pyridine methanols and substituted methanols are prepared which correspond to the formula: ##STR1## wherein X independently represents alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, alkylthio of 1 to 4 carbon atoms, alkylsulfonyl of 1 |
| 4163787 |
Substituted pyridine methyl esters of cyclopropane carboxylic acids and their use as insecticide |
August 7, 1979 |
| Substituted pyridine methyl esters of cyclopropane carboxylic acids and the geometric and optical isomers thereof are prepared which correspond to the formula: ##STR1## wherein X independently represents alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, alkylthio of 1 |
