Abstract: Disclosed are compounds having the formula: ##STR1## wherein: m=0, 1;n=0, 1;Z=CH, N;R.sub.1 is selected from chlorine, bromine, fluorine, CF.sub.3, phenyl, C.sub.1 -C.sub.2 -alkoxy, C.sub.1 -C.sub.2 -haloalkoxy, alkylthio, and haloalkylthio, wherein the halogen is Cl, Br, F;R.sub.2 is H, fluorine, chlorine, or bromine;R.sub.3 represents H, CH.sub.3, CN, or also F when m=1 or when n=1 and R.sub.4, R.sub.5 are H;R.sub.4, R.sub.5 are independently H or F;R.sub.3 and R.sub.4, furthermore, when m=0, may represent, taken together, a second bond between the two carbon atoms to which they are linked in formula (I); andR.sub.f is selected from the group consisting of polyfluoroalkyls, polyfluoroalkenyls and polyfluoroalkynyls containing up to 4 carbon atoms, containing at least 2 F atoms and, optionally, other halogens selected from Cl and Br.Anti-fungal compositions containing these new compounds.

Abstract: Nitrogen-containing heterocyclic compounds endowed with antifungal action, which have the general formula: ##STR1## wherein: Ar=phenyl, optionally substituted with halogens, (C.sub.1 -C.sub.3)-alkyls, (C.sub.1 -C.sub.3)-haloalkyls, (C.sub.2 -C.sub.4)-alkenyls, (C.sub.2 -C.sub.4)-haloalkenyls, (C.sub.1 -C.sub.3)-alkoxy groups, (C.sub.1 -C.sub.4)-haloalkoxy groups; pyridyl, optionally substituted with one or more halogens or with (C.sub.1 -C.sub.3)-haloalkyls;K, X, Z=O or S;B.sub.1, B.sub.2 =(C.sub.1 -C.sub.6)-alkylidenes;Rhl=(C.sub.1 -C.sub.6)-haloalkyl, (C.sub.2 -C.sub.8)-haloalkenyl, (C.sub.3 -C.sub.8)-haloalkoxyalkyls, (C.sub.3 -C.sub.8)-haloalkoxyalkenyls;A represents a group selected from among ##STR2## wherein; R.sub.1, R.sub.2, R.sub.3 =H, (C.sub.1 -C.sub.6)-alkyls, (C.sub.1 -C.sub.6)-haloalkyls, (C.sub.2 -C.sub.6)-alkenyls, (C.sub.2 -C.sub.6)-haloalkenyls, (C.sub.2 -C.sub.6)-alkinyls, (C.sub.2 -C.sub.6)-haloalkinyls; andG=CH or N.

Abstract: Disclosed are compounds, having the general formula: ##STR1## wherein: m=0, 1, 2; n=0, 1 with the condition that when m=0, also n=0;p=0, 1; q=1, 2;X is either oxygen or sulphur;A=N, CH;R is H, CH.sub.3, F;R.sub.1 is selected from chlorine, bromine, fluorine, CF.sub.3, phe=nyl, C.sub.1 -C.sub.2 -alkoxy, C.sub.1 -C.sub.2 -haloalkoxy, alkylthio, haloalkyl=thio, wherein the halogen is Cl, Br, F;R.sub.2 is selected from H, chlorine, bromine, fluorine;R.sub.f is selected from the group formed by alkyls containing from 2 to 4 carbon atoms, and containing at least 4 atoms of halogen selected from F, Cl and Br, of which at least 3 are F atoms; alkenyls and alkynyls containing up to 4 carbon atoms, containing at least 2 F atoms and, optionally, other halogens selected between Cl and Br.

Abstract: There are described compounds having general formula: ##STR1## wherein: R.sup.1 is selected from the group comprising F, Cl, Br, CF.sub.3, a phenyl, a C.sub.1 -C.sub.2 alkoxy, a C.sub.1 -C.sub.2 haloalkoxy, an alkylthio, a haloalkylthio radical, in which the halogen is F, Cl, Br;R.sup.2 is selected from the group comprising H, F, Cl, Br, CF.sub.3 ;R.sup.3, R.sup.4 and R.sup.5, which may be the same or different, are H, a C.sub.1 -C.sub.4 alkyl or a C.sub.3 -C.sub.6 cycloalkyl radical, on condition that R.sup.5 is different from R.sup.3, when R.sup.4 is H;Y is selected from the group comprising H, CH.sub.3, OH, CN, F;n is 1,2;m is 0,1;X is O or S;Rf is selected from the group consisting of C.sub.1 -C.sub.5 polyfluoroalkyl, C.sub.2 -C.sub.4 polyfluoroalkenyl, polyfluoroalkoxyalkyl and polyfluoroalkoxyalkenyl radicals, everyone of them containing at least two fluorine atoms and, optionally, other halogen atoms selected from Cl and Br;Z is CH or N.

Abstract: Fungicidal compounds having the formula: ##STR1## wherein: R.sup.1 is selected from the group consisting of F, Cl, Br, CF.sub.3, a phenyl, a C.sub.1 -C.sub.2 alkoxy, a C.sub.1 -C.sub.2 haloalkoxy, an alkylthio, and a haloalkylthio radical, in which the halogen is F, Cl, or Br;R.sup.2 is selected from the group consisting of H, F, Cl, Br, and CF.sub.3 ;R.sup.3 is H, a C.sub.1 -C.sub.4 alkyl or a C.sub.3 -C.sub.6 cycloalkyl radical;Y is selected from the group consisting of H, CH.sub.3, OH, CN, and F;n is 1, 2, 3, 4 with the proviso that Y is OH when n is 1;m is 0 or 1;X is O or S;Rf is selected from the group consisting of C.sub.1 -C.sub.5 polyfluoroalkyl, C.sub.2 -C.sub.4 polyfluoroalkenyl, polyfluoroalkoxyalkyl and polyfluoroalkoxyalkenyl radicals, each one of them containing at least two fluorine atoms and, optionally, other halogen atoms selected from the group consisting of Cl and Br; andZ is CH or N.

Abstract: A method of fighting fungus infections by using compounds having the formula: ##STR1## wherein: R is H, a C.sub.1 -C.sub.4 alkyl, an alkenyl, or an alkynyl radical; n is 1 or 2;A represents a C.sub.1 -C.sub.6 alkylene bridge, an arylene or a heterocyclic bridge;X represents O, S, SO, SO.sub.2 ; andR.sup.1 is selected from the group consisting of C.sub.1 -C.sub.6 alkyl radicals, a phenyl radical, optionally substituted, polyfluoroalkyl radicals containing from 1 to 4 carbon atoms and at least 2 fluorine atoms, polyfluoroalkenyl radicals containing from 2 to 4 carbon atoms and at least 2 fluorine atoms, but excluding compounds having the formula (I) wherein A is an alkylene radical, n is 2, and R.sup.1 is a C.sub.1 -C.sub.6 alkyl radical.

Abstract: There are described compounds exerting an antidotal activity belonging to the classes of the 2-thiazolines-2-substituted and 2-oxazolines-2-substituted, useful in the defense of agrarian cultivations from the toxic action of non-selective herbicides. Utilization and preparation methods thereof are described as well.

Abstract: This invention relates to novel compounds having antidotal activity so as to be useful in the protection of cultivations of agrarian interest from the toxic action of non-selective weed-killers. The novel compounds of this invention have the formula: ##STR1## wherein R=alkyl, phenyl; R.sup.1 =OR.sup.4 =alkyl, cycloalkyl, cyclohexylmethyl, allyl, propargyl, phenyl or benzyl, optionally substituted; R.sup.2 =H or R.sup.1 and R.sup.2 together form a bond between carbonyl and the nitrogen atom which they are linked to; X=O, S; R.sup.3 is the same are R.sup.4, but is different from 3,5-dichlorophenyl.

Abstract: There are disclosed compounds having the formula (I) and (II): ##STR1## wherein: R' and R", equal to or different from each other, are a C.sub.1 -C.sub.7 alkyl, a C.sub.3 -C.sub.7 cycloalkyl, a heterocycloalkyl, alkoxyalkyl, dialkoxyalkyl, haloalkyl;X is a halogen, a C.sub.1 -C.sub.4 alkyl, a haloalkyl, alkoxyl, phenyl; andY is H or a halogen.

Abstract: There are disclosed compounds having general formula (I): ##STR1## wherein: X is H, a phenyl, phenylalkyl, phenylcarbonyl, phenyloxy group, optionally substituted with a halogen; Y is N or CH; R.sup.1 is H or a phenyl group; R.sup.2 and R.sup.3, equal or different, are H, an alkyl, alkoxy group or together they are an atom of ketonic oxygen; R.sup.4 and R.sup.5, equal or different, are H or an alkyl group; R.sup.6 and R.sup.7, equal or different, are H, an alkyl group or one of them forms with R.sup.2 or R.sup.3 an alkylidenic or etheric bridge; or they form a dioxyalkylidenic or alkylidenic ring; m=0, 1; n=0, 1, 2, 3. The compounds are endowed with fungicide and systemic properties.

Abstract: Described herein are .alpha.-(1-triazolyl)-keto-derivatives of general formula: ##STR1## wherein R is phenyl or heteroaryl, optionally substituted, alkyl; R.sup.1 is alkoxyl, optionally substituted aryloxy, alkyl, alkenyl, alkynyl, alkoxyalkyl, alkoxycarbonyl, cyano, optionally substituted phenyl, or, along with R.sup.2, an alkylidene; R.sup.2 is H or, along with R.sup.1, an alkylidene; R.sup.3 is alkylcarbonyl, alkoxycarbonyl, arylcarbonyl, cyano or alkoxyalkylcarbonyl; such compounds being endowed with a high fungicidal activity.

Abstract: A method of protecting useful cultivations from the toxic action of nonselective herbicides, consisting in using, as antidotes, 2- or 4-thiazolidine-carboxylic acids and derivatives thereof.

Abstract: There are described compounds exerting an antidotal activity belonging to the classes of the 2-thiazolines-2-substituted and 2-oxazolines-2-substituted, useful in the defense of agrarian cultivations from the toxic action of non-selective herbicides. Utilization and preparation methods thereof are described as well.

Abstract: Compounds having antidote activity and belonging to the class of the derivatives of 1,3-thiazolidine useful for protecting cultivations of agrarian interest from the toxic action of nonselective herbicides are herein described. The invention relates, also, to a method for protecting cultivations of agrarian interest from the toxic action of nonselective herbicides consisting in the use, as antidotes, of the above mentioned compounds and the compositions for agrarian use containing said compounds.

Abstract: Acyl anilines are disclosed having the formula ##STR1## wherein R and R.sup.1 (like or unlike each other)=H; CH.sub.3 ; C.sub.2 H.sub.5 ; n.C.sub.3 H.sub.7 ; --CH.sub.2 --CH.dbd.CH.sub.2 ; --CH.dbd.CH--CH.sub.3 ;R.sup.3 and R.sup.4 (like or unlike each other)=H; alkyl C.sub.1 -C.sub.3 ; halomethyl; Cl; F; CN; O-alkyl; S-alkyl; alkoxymethyl; orR.sup.3 and R.sup.4 together are (CH.sub.2 .dbd.) ##STR2## n=0,1 Z=phenyl optionally substituted; ##STR3## And R.sup.2 =H, CH.sub.3 ; m=1,2; Y=alkynyl C.sub.2 -C.sub.8 ; phenyl optionally substituted; phenyl-acetyl; furyl, thienyl; pyridyl; heterocyclic groups containing 2 or 3 heteroatoms, one of them different from nitrogen;R.sup.8 =CH.sub.3 ; alkoxymethyl; halomethyl; O-alkyl.The compounds of formula I are endowed with a high fungicidal activity and with a low phytotoxicity.

Abstract: Acyl anilines are disclosed having the formula ##STR1## wherein R and R.sup.1 (like or unlike each other)=H; CH.sub.3 ; C.sub.2 H.sub.5 ; n.C.sub.3 H.sub.7 ; --CH.sub.2 --CH.dbd.CH.sub.2 ; --CH.dbd.CH--CH.sub.3 ;R.sup.3 and R.sup.4 (like or unlike each other)=H; alkyl C.sub.1 -C.sub.3 ; halomethyl; Cl; F; CN; O-alkyl; S-alkyl; alkoxymethyl;or R.sup.3 and R.sup.4 together are (CH.sub.2 .dbd.) ##STR2## (R.sup.9 =alkyl C.sub.1 -C.sub.3); CN; --CH(OR.sup.5).sub.2 (R.sup.5 =alkyl or alkylidene ); ##STR3## (R.sup.6 and R.sup.7 =H, alkyl) `n=0,1 Z=phenyl optionally substituted; ##STR4## And R.sup.2 =H, CH.sub.3 ; m=1,2; Y=alkynyl C.sub.2 -C.sub.8 ; phenyl optionally substituted; phenyl-acetyl; furyl, thienyl; pyridyl; heterocyclic groups containing 2 or 3 heteroatoms, one of them different from nitrogen;R.sup.8 =CH.sub.3 ; alkoxymethyl; halomethy; O-alkyl.The compounds of formula I are endowed with a high fungicidal activity and with a low phytotoxicity.

Abstract: Chloroacetanilides are disclosed having the general formula: ##STR1## wherein R.sup.1 =H, or alkyl with 1-5 carbon atoms, or X;X=alkenyl, and preferably ##STR2## in which the various R.sup.2, which may be equal to or different from each other, are H or an alkyl with 1-3 carbon atoms;A=alkylene, optionally substituted, of the formula: ##STR3## in which the various R.sup.2, which may be equal to or different from each other, have the meanings specified above; andY=H; alkyl with 1-5 carbon atoms; alkenyl with 2-5 carbon atoms; alkinyl with 2-5 carbon atoms; phenyl; cycloalkyl with 3-8 carbon atoms; halogen; ##STR4## wherein R=H; alkyl with 1-5 carbon atoms; alkenyl or alkinyl with 2-5 carbon atoms; cycloalkyl with 3-8 carbon atoms; phenyl;The chloroacetanilide derivatives are useful in combatting infestations of infesting monocotyledons and dicotyledons during pre-emergence, by spreading the chloroacetanilide derivative on the soil adjacent thereto in quantities ranging from 0.25 kg/ha upwards.