| Patent Number |
Title Of Patent |
Date Issued |
| RE40332 |
Fungicidal trifluoromethylalkylamino-triazolopyrimidines |
May 20, 2008 |
| The novel compounds of formula I: ##STR00001## wherein (R.sup.1, R.sup.2, Hal and L.sup.1 through L.sup.5 are defined in the specification) show selective fungicidal activity. The new compounds may be processed with carriers and adjuvants to produce fungicidal compositions. |
| RE35985 |
Fungicidal compositions |
December 8, 1998 |
| The invention provides a fungicidal composition comprising at least one systemic, contact and/or soil fungicide and at least one acrylic acid morpholide derivative of the general formula ##STR1## in which R.sub.1 represents a hydrogen, chlorine or bromine atom, a trifluoromethyl, |
| 7329663 |
Substituted-triazolopyrimidines as anticancer agents |
February 12, 2008 |
| The invention provides a method of treating or inhibiting the growth of cancerous tumor cells and associated diseases in a mammal in need thereof which comprises administering to said mammal an effective amount of a substituted triazolopyrimidine derivative or a pharmaceutically acce |
| 7105664 |
5-Halogen-6-phenyl-7-fluoroalkylamino-triazolopyrimidines as fungicides |
September 12, 2006 |
| 5-Halogen-6-phenyl-7-fluoroalkylamino-triazolopyrimidines of formula I: (I) in which R.sup.1 is hydrogen, fluoro, alkyl, alkenyl, alkynyl, alkadienyl, where the carbon chains of these radicals may be unsubstituted or substituted as defined in the description; R.sup.2 is hydrogen, alk |
| 7084146 |
Fungicidal trifluoromethylalkylamino-triazolopyrimidines |
August 1, 2006 |
| The novel compounds of formula I: ##STR00001## wherein R.sup.1 is hydrogen or methyl; R.sup.2 is hydrogen, or an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl or phenyl group; Hal is halogen; and L.sup.1 through L.sup.5 are each hydrogen, halogen, alkyl, alkoxy or nitro |
| 6380202 |
Fungicidal fluoro-substituted 7-heterocyclyl-triazolopyrimidines |
April 30, 2002 |
| The novel compounds of formula I: ##STR1##wherein (R.sup.1, R.sup.2, Hal and L.sup.1 through L.sup.5 are defined in the specification) show selective fungicidal activity and high systemicity. The new compounds are processed with carriers and adjuvants to fungicidal compositions. |
| 6297251 |
Fungicidal trifluorophenyl-triazolopyrimidines |
October 2, 2001 |
| The novel compounds of formula I: ##STR1##(R.sup.1, R.sup.2 and Hal are defined in the specification) show selective fungicidal activity. The new compounds are processed with carriers and adjuvants to fungicidal compositions. |
| 6255309 |
Fungicidal trifluoromethylalkylamino-triazolopyrimidines |
July 3, 2001 |
| The novel compounds of formula I: ##STR1##wherein (R.sup.1, R.sup.2, Hal and L.sup.1 through L.sup.5 are defined in the specification) show selective fungicidal activity. The new compounds may be processed with carriers and adjuvants to produce fungicidal compositions. |
| 6204269 |
Fungicidal trifluoromethylalkylamino-triazolopyrimidines |
March 20, 2001 |
| The novel optically active compounds of formula I: ##STR1##(R.sup.1, Hal and L.sup.1 through L.sup.5 are defined in the specification) wherein the enantiomeric excess of the (S)-enantiomer is at least 70%., show enhanced selective fungicidal activity. The new compounds are processed |
| 6117876 |
Fungicidal trifluorophenyl-triazolopyrimidines |
September 12, 2000 |
| The novel compounds of formula I: ##STR1## (R.sup.1, R.sup.2 and Hal are defined in the specification) show selective fungicidal activity. The new compounds are processed with carriers and adjuvants to fungicidal compositions. |
| 6020338 |
Fungicidal 7-alkyl-triazolopyrimidines |
February 1, 2000 |
| The novel compounds of formula I: whereinR.sup.1 represents an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl, or aryl group, or an optionally substituted cycloalkyl or cycloalkenyl group, in which one CH.sub.2 group may also be replaced by O, S or NR.sup.2, in which R.sup.2 |
| 5986135 |
Fungicidal trifluoromethylalkylamino-triazolopyrimidines |
November 16, 1999 |
| An improved process for the preparation of (S)-1,1,1-trifluoroalkyl-2-amines of formula IIIA, ##STR1## where R.sup.1 is a C.sub.1-6 alkyl group, from the corresponding racemic mixture, which process includes treating 1 part by mole of the racemic mixture with approximately 0.3 to |
| 5952496 |
Fungicidal compositions |
September 14, 1999 |
| The invention provides a fungicidal composition comprising at least one systemic, contact and/or soil fungicide and at least one acrylic acid morpholide derivative of the general formula ##STR1## in which R.sub.1 represents a hydrogen, chlorine or bromine atom, a trifluoromethyl, |
| 5948783 |
Fungicidal trifluoromethylalkylamino-triazolopyrimidines |
September 7, 1999 |
| The novel compounds of formula I: ##STR1## wherein R.sup.1, R.sup.2, Hal and L.sup.1 through L.sup.5, are defined in the specification show selective fungicidal activity. |
| 5945567 |
Fungicidal 2-methoxybenzophenones |
August 31, 1999 |
| Substituted benzophenone compounds are disclosed, having the formula: ##STR1## The compounds are useful as fungicides having high systemicities. |
| 5922905 |
5-bromo-2-methoxy-6-alkyl benzoic acids |
July 13, 1999 |
| Substituted benzoic acid compounds are disclosed, having the formula: ##STR1## The compounds find use as intermediates for the production of agricultural fungicides. |
| 5910496 |
Fungicidal compositions |
June 8, 1999 |
| The invention provides a fungicidal composition comprising at least one systemic, contact and/or soil fungicide and at least one acrylic acid morpholide derivative of the general formula ##STR1## in which R.sub.1 represents a hydrogen, chlorine or bromine atom, a trifluoromethyl, |
| 5679866 |
Fungicidal methods, compounds and compositions containing benzophenones |
October 21, 1997 |
| There is provided a method for the control of phytopathogenic fungi and disease caused thereby which comprises contacting said fungi with a fungicidally effective amount of a benzophenone compound of formula I ##STR1## There are further provided benzophenone compounds of formula Ia w |
| 5677303 |
Enolethers and their use as a fungicide |
October 14, 1997 |
| Enolethers and thioenolethers of formula I ##STR1## are disclosed. The compounds are useful for combatting phytopathogenic fungi. |
| 5656630 |
Method of combating fungus |
August 12, 1997 |
| The invention relates to a method of combating fungus which comprises treating plants subject to or subjected to fungal attack, seeds of such plants or the medium in which such plants are growing or are to be grown with the Z-isomer of 4-[3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acr |
| 5593996 |
Triazolopyrimidine derivatives |
January 14, 1997 |
| This invention relates to certain triazolopyrimidine derivatives of formula I ##STR1## wherein R.sub.1 represents an optionally substituted alkyl, alkenyl, alkynyl, alkadienyl, cycloalkyl, bicycloalkyl or heterocyclyl group; R.sub.2 represents a hydrogen atom or an alkyl group; o |
| 5399559 |
Fungicidal indole derivatives |
March 21, 1995 |
| The invention relates to fungicidal compositions which comprise a carrier and, as active ingredient, an indole derivative of the formula ##STR1## in which R is a substituted phenyl group; R.sup.3 and R.sup.4 independently are hydrogen or halogen or an optionally substituted alkyl, |
| 5336671 |
Fungicidal compositions containing benzyl-tris(aryl)phosphonium salts |
August 9, 1994 |
| The invention provides fungicidal compositions containing benzyl-tris(aryl)-phosphonium salts of the general formula ##STR1## in which R.sup.1 represents an optionally substituted alkyl or alkoxy group; R.sup.2 represents a hydrogen atom or an optionally substituted alkyl group; |
| 5304376 |
Fungicidal composition |
April 19, 1994 |
| A fungicidal composition in particulate or powder form wherein each active particle thereof comprises a fungicidally active compound, especially an acrylamide such as dimethomorph, dispersed in a polymer material having a melting point below the degradation temperature of the compound. T |
| 5262414 |
Fungicidal compositions |
November 16, 1993 |
| The invention provides a fungicidal composition comprising at least one systemic, contact and/or soil fungicide and at least one acrylic acid morpholide derivative of the general formula ##STR1## in which R.sub.1 represents a hydrogen, chlorine or bromine atom, a trifluoromethyl, |
| 5189035 |
Fungicidal furanone derivatives |
February 23, 1993 |
| The invention provides furanone derivatives of the general formula ##STR1## in which R.sup.1 represents a halogen atom or an optionally substituted alkyl or alkoxy group, R.sup.2 represents a halogen atom or an optionally substituted alkyl, aryl or heterocyclyl group, R.sup.7 represe |
| 5157028 |
Fungicidal compositions |
October 20, 1992 |
| The invention provides a fungicidal composition comprising at least one systemic, contact and/or soil fungicide and at least one acrylic acid morpholide derivative of the general formula ##STR1## in which R.sub.1 represents a hydrogen, chlorine or bromine atom, a trifluoromethyl, |
| 4933328 |
Phosphonium salts and fungicidal use |
June 12, 1990 |
| The invention provides fungicidal compositions containing phosphonium salts of formula: ##STR1## in which n represents 0, 1, 2 or 3, R represents a halogen atom or an optionally substituted alkyl, haloalkyl, alkoxy or haloalkyl group, R.sup.1, R.sup.2 and R.sup.3 independently re |
| 4923866 |
Fungicidal compositions |
May 8, 1990 |
| The invention provides a fungicidal composition comprising at least one systemic, contact and/or soil fungicide and at least one acrylic acid morpholide derivative of the general formula ##STR1## in which R.sub.1 represents a hydrogen, chlorine or bromine atom, a trifluoromethyl, |
| 4910200 |
Acrylic acid morpholides, fungicidal compositions and use |
March 20, 1990 |
| Compounds of the formula ##STR1## wherein A is ##STR2## B is ##STR3## R.sup.1 is hydrogen; halogen, cyano or optionally substituted C.sub.1-4 alkyl; andQ is NR.sup.8 R.sup.9 or ##STR4## where R.sup.2 to R.sup.11 are substituents of various types. The compounds |
