Claims
- 1. A compound having the structural formula ##STR22## where Z is oxygen and Z.sup.1 is sulfur, SO, or SO.sub.2 ; Y is nitrogen or CH; R is linear or branched C.sub.2 -C.sub.12 alkylene; R.sup.1 is hydrogen, C.sub.1 -C.sub.4 alkyl, benzyl or phenyl; R.sup.2 is phenyl, phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl, phenylamino, benzyl, phenoxy substituted with halo, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, nitro, cyano, trihalomethyl or mono-, di- or trihalomethoxy or phenyl substituted with halo, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, nitro, cyano, trihalomethyl or mono-, di- or trihalomethoxy.
- 2. A compound in accordance with claim 1 where Y is nitrogen; Z is oxygen; Z.sup.1 is sulfur or SO.sub.2 ; R is linear or branched C.sub.2 -C.sub.5 alkylene; R.sup.1 is hydrogen, methyl or phenyl; and R.sup.2 is phenyl, phenylthio, phenoxy, phenyl substituted with fluorine, chlorine, bromine, methyl, methoxy, trifluoromethyl or dichloromethoxy or phenoxy substituted with fluorine, chlorine, bromine, methyl, methoxy, trifluoromethyl or dichloromethoxy.
- 3. A compound in accordance with claim 2 wherein R is C.sub.2 alkylene; R.sup.1 is hydrogen; and R.sup.2 is phenyl, phenylthio, phenoxy, phenyl substituted with bromine or phenoxy substituted with bromine.
- 4. A process for controlling fungi which comprises applying a fungicidally effective amount of the compound of claim 1.
- 5. A process for controlling fungi which comprises applying a fungicidally effective amount of the compound of claim 2.
- 6. A process for controlling fungi which comprises applying a fungicidally effective amount of the compound of claim 3.
- 7. A fungicidal composition comprising:
- (a) a fungicidally effective amount of a compound having the structural formula: ##STR23## wherein: Z is oxygen and Z.sup.1 is sulfur, SO, or SO.sub.2
- Y is nitrogen or CH;
- R is a linear or branched C.sub.2 -C.sub.12 alkylene;
- R.sup.1 is hydrogen, C.sub.1 -C.sub.4 alkyl, benzyl or phenyl;
- R.sup.2 is phenyl; phenoxy; phenylthio; phenylsulfinyl; phenylsulfonyl; phenylamino; benzyl; phenoxy substituted with halo, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, nitro, cyano, trihalomethyl or mono-, di- or trihalomethoxy; or phenyl substituted with halo, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, nitro, cyano, trihalomethyl or mono-, di or trihalomethoxy; and
- (b) at least one member of the group consisting of solid inert carriers and liquid inert carriers.
- 8. A fungicidal composition in accordance with claim 7 wherein, in component (a)
- Y is nitrogen;
- Z is oxygen;
- Z.sub.1 is sulfur or SO.sub.2 ;
- R is linear or branched C.sub.2 -C.sub.5 alkylene;
- R.sup.1 is hydrogen, methyl or phenyl; and
- R.sup.2 is phenyl; phenylthio; phenoxy; phenyl substituted with fluorine, chlorine, bromine, methyl, methoxy, trifluoromethyl or dichloromethoxy; or phenoxy substituted with fluorine, chlorine, bromine, methyl, methoxy, trifluoromethyl or dichloromethoxy.
- 9. A fungicidal composition in accordance with claim 8 wherein, in component (a)
- R is C.sub.2 alkylene;
- R.sup.1 is hydrogen; and
- R.sup.2 is phenyl, phenylthio, phenoxy, phenyl substituted with bromine or phenoxy substituted with bromine.
REFERENCE TO RELATED APPLICATION
This is a continuation-in-part application of U.S. patent application, Ser. No. 606,025 filed May 2, 1984, now abandoned.
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Dec 1982 |
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4479004 |
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4559355 |
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Continuation in Parts (1)
|
Number |
Date |
Country |
Parent |
606025 |
May 1984 |
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