5-Aminomethyl-1,3-oxathiolane microbicides, compositions and use
AssigneeBayer Aktiengesellschaft
InventorsJoachim Weissmuller, Wolfgang Kramer, Dieter Berg, Paul Reinecke, Wilhelm Brandes, Gerd Hanssler
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AssigneeBayer Aktiengesellschaft
InventorsJoachim Weissmuller, Wolfgang Kramer, Dieter Berg, Paul Reinecke, Wilhelm Brandes, Gerd Hanssler
Estimating the term…
MIcrobicidally active 5-aminomethyl-1,3-oxathiolanes of the formula ##STR1## in which R.sup.1 is tetrahydronaphthyl, decahydronaphthyl or optionally substituted naphthyl, optionally substituted cycloalkyl or cycloalkenyl, optionally substituted phenyl, or alkyl which is substituted by phenyl, phenoxy, phenylthio, cyclohexyl, cyclohexyloxy or cyclohexylthio, each of which is optionally substituted, R.sup.2 is hydrogen or methyl, R.sup.3 is alkyl, and R.sup.4 is alkyl, alkenyl or optionally substituted aralkyl, or R.sup.3 and R.sup.4, together with the nitrogen atom to which they are bonded, form an optionally substituted saturated heterocyclic structure which can contain further heteroatoms, or a plant-tolerated addition product thereof with an acid or metal salt.
A 5-aminomethyl-1,3-oxathiolane of the formula ##STR183## in which R.sup.1 is tetrahydronaphthyl, decahydronaphthyl or optionally substituted naphthyl, optionally substituted cycloalkyl or cycloalkenyl, optionally substituted phenyl, or alkyl which is substituted by phenyl, phenoxy, phenylthio, cyclohexyl, cyclohexyloxy or cyclohexylthio, each of which is optionally substituted,
Dependencies are inferred from the claim text.