ПРИМЕНЕНИЕ ЗАМЕЩЕННЫХ СПИРОЦИКЛИЧЕСКИХ СУЛЬФОНАМИДОКАРБОНОВЫХ КИСЛОТ, СЛОЖНЫХ ЭФИРОВ ЗАМЕЩЕННЫХ СПИРОЦИКЛИЧЕСКИХ СУЛЬФОНАМИДОКАРБОНОВЫХ КИСЛОТ, АМИДОВ ЗАМЕЩЕННЫХ СПИРОЦИКЛИЧЕСКИХ СУЛЬФОНАМИДОКАРБОНОВЫХ КИСЛОТ И ЗАМЕЩЕННЫХ СПИРОЦИКЛИЧЕСКИХ СУЛЬФОНАМИДОКАРБОНИТРИЛОВ ИЛИ ИХ СОЛЕЙ ДЛЯ ПОВЫШЕНИЯ ТОЛЕРАНТНОСТИ РАСТЕНИЙ К СТРЕССУ
1. Use of substituted spirocyclic sulfonamidokarbonovyh acids, esters of substituted spirocyclic sulfonamidokarbonovyh acids, amides of substituted spirocyclic sulfonamidokarbonovyh acids and substituted spirocyclic sulfonamidokarbonitrilov general formula (I) or their soleydlya increasing plant tolerance to abiotic stress, gdeQ represents a group Q-6-Q-11prichem a-a, r and residues RR, and Y in each case have the meanings as defined below, wherein the arrow represents a bond to the sulfur atom of SO , A, A, Ayavlyayutsya same or different and each independently represent N (nitrogen atom) or a CW group, where, in any case, more than two nitrogen atoms may not be adjacent, and wherein W in CW group in each case have identical or different values, as disclosed hereinafter, W in each case is hydrogen, nitro, amino, cyano, thiocyanato, isothiocyanato, halogen, (CC) -alkyl, (CC) -cycloalkyl, (CC) -alkenyl, ( CC) -alkynyl, aryl, aryl- (CC) -alkyl, aryl- (CC) alkoxy, heteroaryl, (CC) -alkoxy- (CC) -alkyl, (CC) -galoalkil, (CC) galotsikloalkil, (CC ) - lkoksi, (CC) -galoalkoksi, aryloxy, heteroaryloxy, (CC) -tsikloalkiloksi, (CC) -cycloalkyl- (CC) -alkoxy, (CC) -alkoxycarbonyl, hydroxycarbonyl, aminocarbonyl, (CC) -alkylaminocarbonyl, (CC) - tsikloalkilaminokarbonil, cyano (CC) -alkylaminocarbonyl, (CC) -alkenilaminokarbonil, (CC) -alkinilaminokarbonil, (CC) alkylamino, (CC) -alkylthio, (CC) -galoalkiltio, bis (CC) alkylamino, (CC ) -tsikloalkilamino, (CC) -alkilkarbonilamino, (CC) -tsikloalkilkarbonilamino, formylamino, (CC) -galoalkilkarbonilamino, (CC) -alkoksikarbonilamino, (CC) -alkilaminokarbonilamino, [(CC) alkyl] -s