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| Number | Title | Issue Date |
| 7282068 | Polycationic azo compounds for dyeing keratin fibers, dye composition containing the same, and methods for making such compounds The present disclosure relates to compounds used as direct dyes, and dyeing compositions comprising such compounds. The disclosed compounds have the formula A-L-B, wherein A and B are chosen from arylazoimidazolium coloring functional groups, and L is a linker compr... | 10/16/2007 |
| 6906085 | Tetrahydropyran derivatives as neurokinin receptor antagonists The present invention relates compounds of the formula (I): wherein R1, R2, R3, R4, R5, R6, R7 and R8 represent a variety of subst... | 06/14/2005 |
| 6376497 | Antifungal azole derivatives having a fluorinated vinyl group and process for preparing same An antifungal compound of formula (I) or a pharmaceutically acceptable salt thereof: ##STR1## wherein: X is CH or N; Y is O, ##STR2## R1 and R2 are each independently F or Cl; R3 is a thiophenyl, naphthyl, or phenyl group,... | 04/23/2002 |
| 5872258 | Commercial process for the manufacture of fluconazole and intermediates useful in the manufacture thereof A process for making Fluconazole is provided comprising carrying out the following scheme of reaction: ##STR1##... | 02/16/1999 |
| 5750719 | Commercial process for the manufacture of fluconazole and intermediates useful in the manufacture thereof A process for making Fluconazole is provided comprising carrying out the following scheme of reaction: ##STR1##... | 05/12/1998 |
| 5710154 | Tetrahydrofuran antifungals A compound represented by the formula I ##STR1## wherein X is independently both F or both Cl or one X is independently F and the other is independently Cl; R1 is a straight or branched chain (C3 to C8) alkyl group su... | 01/20/1998 |
| 5693626 | Tetrahydrofuran antifungals A compound represented by the formula I ##STR1## wherein X is independently both F or both Cl or one X is independently F and the other is independently Cl; R1 is a straight or branched chain (C3 to C8) alkyl group su... | 12/02/1997 |
| 5661151 | Tetrahydrofuran antifungals A compound represented by the formula I ##STR1## wherein X is independently both F or both Cl or one X is independently F and the other is independently Cl; R1 is a straight or branched chain (C3 to C8) alkyl group su... | 08/26/1997 |
| 5486625 | Process for the preparation of chiral intermediates useful for the synthesis of antifungal agents Described is a process for preparing chiral compounds of the formula ##STR1## wherein X1 and X2 are independently F or Cl, and Y is Cl, Br or I, comprising reacting a triol of the formula ##STR2## wherein X1 and ... | 01/23/1996 |
| 5476845 | Use of phosphoric esters as crystallization inhibitors A new process for preventing the crystallization of certain azole derivatives in the spray equipment upon spraying mixtures containing A) certain azole derivatives which have a tendency to crystallize and B) if appropriate one or more other active compounds and add... | 12/19/1995 |
| 5466821 | Heterocyclic compounds Fungicidal triazole and imidazole compounds are disclosed. Intermediate for preparing these compounds include, for example, compounds of the formula: ##STR1## wherein R1 is phenyl optionally substituted by halogen, nitro, alkyl, haloalkyl,... | 11/14/1995 |
| 5432190 | Pharmaceutical compositions containing triazoles and method of treating estrogen-dependent diseases Azole derivatives (including stereoisomers and pharmaceutically acceptable salts) of the formula: ##STR1## wherein R1 and R2 each are H or C1 -C4 alkyl; R3 is H, OH, CN, halogen, haloalkyl, C | 07/11/1995 |
| 5403937 | Process for preparing intermediates for the synthesis of antifungal agents Disclosed is a process for preparing chiral compounds of the formula (I) ##STR1## wherein: X1 and X2 are independently F or Cl; and E is --SO2 R2, wherein R2 is C1 -C6 alkyl, --C... | 04/04/1995 |
| 5395942 | Heterocyclic compounds Triazole and imidazole compounds having the general formula (I): ##STR1## wherein R1 and R2, which may be the same or different, are hydrogen, alkyl, optionally unsubstituted cycloalkyl, cycloalkylmethyl, alkenyl, heterocyclyl, ... | 03/07/1995 |
| 5380741 | Fungicidal triazole and imidazole derivatives The invention relates to new compounds containing a triazole or imidazole group having plant protection use of general formula: ##STR1## in which: W is N or CH; E is CH2 or O; X is a halogen or an alkyl radical; n is an integer from 0 to 5; R | 01/10/1995 |
| 5371065 | Substituted azolylmethyloxiranes Fungicidal and plant growth-regulating substituted azolylmethyloxiranes of the formula ##STR1## in which R1 stands for alkyl, R2 stands for alkyl, X stands for a nitrogen atom or the CH group, Y stands (or halogen, alkyl, cycloalkyl,... | 12/06/1994 |
| 5344834 | Functionalized vinyl azoles and methods of use Pharmaceutical preparations comprising functionalized vinyl azoles of formula I ##STR1## wherein the substituents are as defined herein, including novel compounds, as well as methods of use and methods of their preparation, are provided.... | 09/06/1994 |
| 5266585 | Arylphenyl ether derivatives, compositions containing these compounds and use thereof Arylphenyl ether derivatives of the formula ##STR1## wherein Az is 1H-(1,2,4-triazolyl) or is 1-imidazolyl optionally substituted by alkyl, each of Ra and Rb is hydrogen, halogen, alkyl, alkoxy or nitro, Ar is phenyl or naphthyl, opt... | 11/30/1993 |
| 5245042 | Preparation of cis-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(halopheny)-3-(halophenyl) oxirane A process is described for the preparation of cis-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(halophenyl)-3-(halophenyl)oxirane I ##STR1## by epoxidizing Z-3-(1H-1,2,4-triazol-1-yl)-2-(halophenyl)-1-halophenyl)propene II, ##STR2## where halogen is i... | 09/14/1993 |
| 5225550 | Process for the preparation of substituted acyclic nucleosides, and intermediates occurring therein It is possible, by using symmetrical formaldehyde acetals of the formula ##STR1## in which the substituents R1 -R3 have the specified meanings, advantageously to introduce the substituent ##STR2## into nitrogen-containing h... | 07/06/1993 |
| 5225430 | Azolylmethyloxabicyclohexane derivatives and fungicidal compositions thereof Disclosed herein is a process for preparing a cis-azole derivative represented by the general formula (I) ##STR1## wherein R1 and R2 denote each a hydrogen atom or an alkyl group, R denotes a halogen atom, a nitro group, a cyano... | 07/06/1993 |
| 5210198 | Fungicides containing triazole and oligoether groups Fungicides, which can be used especially against diseases of cereals, of formula: ##STR1## in which: x is a halogen atom or a cyano or nitro group or an alkyl or alkoxy group, optionally halogenated, n is a positive integer, or 0, less than 6, W deno... | 05/11/1993 |
| 5134152 | Oxetane derivatives and their use as anti-fungal or fungicidal agents Compounds of formula (I): ##STR1## [in which: R1 and R2 are hydrogen or alkyl, or together are cycloalkyl; R3 and R4 are hydrogen, alkyl or phenyl, or together are cycloalkyl; or R1 and R3 | 07/28/1992 |
| 5134240 | Bicyclic peroxides Novel 4-substituted-4,8-dimethyl-2,3-dioxabicyclo[3.3.1] nonan-7-ones which have a pronounced activity against the causative organism of malaria and can be used for the prevention and control of malaria.... | 07/28/1992 |
| 5104438 | N-oxoazolylmethyloxiranes and fungicides and bioregulators containing them N-Oxoazolylmethyloxiranes of the formula I ##STR1## where A and B are identical or different and each is alkyl, cycloalkyl, tetrahydropyranyl, benzyl, norbornyl, naphthyl, biphenyl or phenyl, these radicals being unsubstituted or substituted, and X i... | 04/14/1992 |
| 5057531 | Azolylmethyloxiranes and fungicides containing these compounds Azolylmethyloxiranes of the general formula I ##STR1## where R1 and R2 are substituted or unsubstituted alkyl, naphthyl, biphenyl, dioxanyl or phenyl, m and n are each an integer from 1 to 5 or 0, with the proviso that m+n is 1 ... | 10/15/1991 |
| 5049573 | Fungicidal substituted triazoles Fungicidal trazoles of the formula ##STR1## in which Ar stands for optionally substituted aryl, A stands for the groups ##STR2## and X stands for the groups ##STR3## wherein R1 stands for hydrogen or alkyl, R2 stands... | 09/17/1991 |
| 5039332 | Substituted oxathiolanes This invention relates to novel imidazole and triazole substituted oxathiolane compounds and compositions containing said compounds having fungicidal and plant growth regulant activity and methods for preparing same.... | 08/13/1991 |
| 5036094 | Azolyl-derivatives endowed with antifungal activity 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, CH3, F; R1 is selected from chlorine, bro... | 07/30/1991 |
| 5017594 | 1-halo-1-azolylpropenes and -methyloxiranes and fungicides containing these compounds 1-Halo-1-azolylpropenes and -methyloxiranes of the formula I ##STR1## where R1 and R2 are alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, A is oxygen or a single bond, R... | 05/21/1991 |
| 4940799 | Preparation of the diastereomeric mixture 2R,4S-1-[2-(2,4-dichlorophenyl)-4-n-propyl-1,3-dioxolan-2-ylmethyl]-1H-1 ,2,4-triazole The 2R,4S-isomer of formula I and the 2RS,4S-diastereoisomeric mixture of formula Ia of 1-[2-(2,4-dichlorophenyl)-4-n-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-tri azole ##STR1## and the preparation thereof are described. The compounds of formulae... | 07/10/1990 |
| 4939162 | 1-(2-aryl-1,3-dioxon-2-ylmethyl)-1H-imidazoles and 1H-1,2,4-triazoles Novel 1-(2-aryl-1,3-dioxan-2-ylmethyl)-1H-imidazoles and 1H-1,2,4-triazoles wherein the 1,3-dioxane ring is optionally substituted with 1 to 3 substituents.... | 07/03/1990 |
| 4929735 | Process for the preparation of oxiranes A process for the preparation of an oxirane of the formula ##STR1## in which X is 4-chlorobenzyl, 4-phenylphenoxy or 1H-(1,2,4)-triazolyl, comprising reacting dimethyl sulphate with an excess of dimethyl sulphide thereby to form trimethylsulphonium methyl... | 05/29/1990 |
| 4906652 | Azolymethyloxiranes and their use as crop protection agents Compounds of the formula ##STR1## where R, Hal and Z have the meanings given in the disclosure. The compounds are suitable for use as fungicides.... | 03/06/1990 |
| 4883882 | Process for the preparation of compounds containing a triazole and tetrahydrofuran group, and new compounds capable of being employed for the preparation of the said compounds Process for the preparation of compounds containing a triazole and tetrahydrofuran group, and new compounds capable of being employed for the preparation of the said compounds. The invention relates to a process for the preparation of 2-(1-triazolyl)methy... | 11/28/1989 |
| 4870094 | Substituted imidazoles and triazoles A compound of the formula ##STR1## where Z and Z1 are the same or different and are oxygen, sulfur, SO, SO2, or NR3 ; except that Z and Z1 are not simultaneously oxygen, also, if Z or Z1 is sulfu... | 09/26/1989 |
| 4863943 | Fungicides containing triazole and oligoether groups Fungicides, which can be used especially against diseases of cereals, of formula: ##STR1## in which x is a halogen atom or a cyano or nitro group or an alkyl or alkoxy group, optionally halogenated, n is a positive integer, or 0, less than 6, W denot... | 09/05/1989 |
| 4853399 | Microbicidal triazolyl phenylethanone ketals Novel substituted 2-(1H-1,2,4-triazolyl)-1-phenylethan-1-one ketals of the general formula ##STR1## wherein one of the two phenyl substituents is in 2-position and the other is in 4-position, and wherein Ra is halogen, methyl or C1 | 08/01/1989 |
| 4818758 | 2-azolylmethyl-2-phenyl-4-[benzazol-2-yloxy-or-thio-methyl]-1,3 dioxolanes and salts thereof, pharmaceutical compositions containing them and their use Compounds of the formula I ##STR1## and the acid-addition salts thereof, where A=CH or N; Ar=naphthyl, thienyl or phenyl; Z=oxygen or sulfur; R1 =alkyl, F or Cl; g=0-2; L=0 or 1; m=0-4; p=0 or 1; X=O, S or N--R3 ; R2 ... | 04/04/1989 |
| 4810718 | Azolyl-derivatives having fungicidal activity Compounds having the formula: ##STR1## wherein: m=1 or 2; q=1 or 2; Y=a haloethylene or haloethenyl group; X is oxygen or sulfur; A=N or CH; R is H, CH3 or F; R1 is selected from the group comprising chlorine, bromine, fluorine CF | 03/07/1989 |
