The present invention relates to compounds of formula (I), wherein R1, R2, R3, R4 and R5 are as defined in claim 1; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes for preparing compounds of formula (I), to intermediates used in the preparation of compounds of formula (I), to methods of controlling plants and compositions comprising compounds of formula (I).
This invention provides chemical inhibitors of the activity of various phospholipase enzymes, particularly cytosolic phospholipase A
2
enzymes (cPLA
2
), more particularly including inhibitors of cytosolic phospholipase A
2
alpha enzymes (cPLA
2
α). In some embodiments, the inhibitors have the Formula I:
wherein the constituent variables are as defined herein.
This invention provides chemical inhibitors of the activity of various phospholipase enzymes, particularly cytosolic phospholipase A
2
enzymes (cPLA
2
), more particularly including inhibitors of cytosolic phospholipase A
2
alpha enzymes (cPLA
2
α). In some embodiments, the inhibitors have the Formula I:
wherein the constituent variables are as defined herein.
The present invention relates to compounds of formula (I), wherein R
1
, R
2
, R
3
, R
4
and R
5
are as defined in claim
1
; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes for preparing compounds of formula (I), to intermediates used in the preparation of compounds of formula (I), to methods of controlling plants and compositions comprising compounds of formula (I).
Die Erfindung betrifft neuartige substituierte Sulfonylaminoazole der allgemeinen Formel (I)
ein Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide.
Die allgemeine Formel (I) repräsentiert die möglichen Isomeren der Formeln (IA), (IB) und (IC).
sowie Gemische dieser Isomeren.
(In den obigen Formeln haben die variablen Reste R1, R2, R3, R4, A bzw. A', D, E, X, Y und Z die in der Beschreibung angegebenen Bedeutungen).