Control of fungi using phenylpropylammonium salts

Details Control of fungi using phenylpropylammonium salts Control of fungi using phenylpropylammonium salts

1982-08-24

1984-09-18

Bond, Robert T.

Drug, bio-affecting and body treating compositions

Antigen, epitope, or other immunospecific immunoeffector

Parasitic organism or component thereof or substance...

548578, 260239B, 260239BF, 544 581, 544 59, 544173, 544174, 544175, 546216, 546219, 546220, 546221, 546222, 546192, 424244, 424246, 4242484, A61K 31445, C07D21114

Patent

active

044724128

ABSTRACT:
A fungicidal agent contains a phenylpropylammonium salt of the formula ##STR1## where R.sup.1, R.sup.2 and R.sup.3 are each hydrogen, unsubstituted or substituted alkyl, unsubstituted or substituted aryl or aralkyl, cycloalkyl, alkoxy, acyl or halogen, R.sup.4 is alkyl, alkenyl or alkoxy, R.sup.5 is alkyl, alkenyl, alkynyl or unsubstituted or substituted aralkyl, R.sup.6 and R.sup.7 are each hydrogen, alkyl, CH.sub.2 OH or OH, X is CH.sub.2, O, S, C.dbd.O, (CH.sub.2).sub.2 or CH.sub.2 CH--R.sup.8 where R.sup.8 is alkyl, m is 0, 1 or 2, n is 0 or 1 and Y.crclbar. is the anion of a non-phytotoxic acid, with the proviso that the bond represented by the broken line may be hydrogenated if m is 0 or 1, and is always hydrogenated if m is 2.

REFERENCES:
patent: 2842546 (1958-07-01), Lane
patent: 3037910 (1962-06-01), Copp et al.
patent: 4241058 (1980-12-01), Pfiffner
Fieser and Fieser, "Organic Chemistry", 3rd Edition, (1956), (Heath), p. 228.
Stanier et al., "The Microbial World", (1957), (Prentice-Hall), Chapter 5, pp. 76-98.
Chemical Week, Jun. 21, 1972, p. 46.
Wegler, Chemie der Pflanzenschutzund Schadlingsbekampfungsmittel, vol. 4, (1977), pp. 24-26.

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