摘要:
Compounds of the formula I ##STR1## where Ar is unsubstituted or substituted phenyl, pyridyl, thienyl or napthyl,R.sup.1 is hydrogen or CN,R.sup.2 is unsubstituted or substituted aryl, hetaryl, alkyl or cycloalkyl, or is unsubstituted or substituted alkenyl or alkynyl,x is CH.sub.2, O or S andn is 0 or 1,their plant-tolerated acid addition salts and metal complexes, and fungicides and growth regulators containing these compounds.
摘要:
Substituted N-hydroxypyrazoles of the general formula ##STR1## where R.sup.1, R.sup.2 and R.sup.3 are identical or different and are hydrogen, alkyl, haloalkyl, cycloalkyl, alkoxycarbonyl, halogen, aryl or arylalkyl, the aromatic ring being unsubstituted or substituted,or R.sup.2 and R.sup.3 form, with the pyrazole ring, a substituted or unsubstituted aromatic or aliphatic ring,X is CH or N, and their plant-tolerated acid addition salts and metal complexes,and fungicides containing these compounds.
摘要:
Compounds of the general formula I ##STR1## where X is alkyl, aryl, aryloxy or alkoxy, Y is hydrogen, alkyl, alkoxy, halogen, aryl or aryloxy, n is 0 to 5, and Z is CH or N, and fungicides containing these compounds.
摘要:
Compounds of the general formula ##STR1## where 5 R is alkyl or substituted or unsubstituted aryl,X is C.dbd.O or CHOH and derivatives thereof,Y is hydrogen, alkyl, alkoxy, halogen, aryl or aryloxy, andn is 1 to 5,and fungicides containing these compounds.
摘要:
Compounds of the general formula ##STR1## where X is CH.sub.2 or O, Y is hydrogen, alkyl, alkoxy, halogen, aryl or aryloxy and n is from 1 to 5, and their salts and complexes, and fungicides containing these compounds.
摘要:
N-Thiocyanatomethoxyazaheterocycles of the general formula INCS--CH.sub.2 --O--Het(where Het is pyrazolyl, imidazolyl or triazolyl, each of which may be substituted, or is indazolyl, benzoimidazolyl or benzotriazolyl, where each of the fused benzene rings may furthermore be substituted, and the salts and metal complexes thereof, with the exception of 1-[(thiocyanato)methoxy]-pyrazole, and biocides containing them.
摘要:
The preparation of 1-hydroxyimidazoles of the formula I ##STR1## where the R radicals can be identical or different and are each halogen or an organic radical, it also being possible for vicinal radicals to be connected to form an aromatic or nonaromatic ring of from 3 to 12 carbon atoms, and n is from 0 to 3, entails reacting an imidazole of the formula II ##STR2## where Q is preferably hydrogen or, especially where R is not halogen, an alkali metal or alkaline earth metal cation, with an organic peroxide.The 1-hydroxyimidazole and its halogen substituted derivatives of the formula I and the acid addition salts thereof are valuable intermediates for organic syntheses.
摘要:
1-hydroxy-1,2,4-traizoles have the general formula I ##STR1## where R.sup.1 and R.sup.2 are singly independently of the other hydrogen, alkyl, halogen or substituted or unsubstituted aryl or together an alkylene chain.
摘要:
Novel substituted N-hydroxypyrazoles or N-hydroxytriazoles of the general formula I ##STR1## where X and Y are O, S, SO, SO.sub.2 or CH.sub.2, B is N-pyrazolyl or N-1,2,4-triazolyl of the formulae Ba and Bb respectively ##STR2## R.sup.1 and R.sup.2 are hydrogen or C.sub.1 -C.sub.3 -alkyl, R.sup.3 is hydrogen, halogen or C.sub.1 -C.sub.3 -alkyl, z is 1, 2 or 3, R.sup.4, R.sup.5 and R.sup.6 are hydrogen, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkyl or C.sub.1 -C.sub.4 -haloalkoxy, and n is 0, 1 or 2, and methods of combating pests.
摘要:
N-hydroxypyrazoles of the general formula I ##STR1## where R.sup.1, R.sup.2 and R.sup.3 may be identical or different and are each hydrogen or halogen, are prepared by a process in which a pyrazole of the general formula II ##STR2## where R.sup.1, R.sup.2 and R.sup.3 have the meanings stated for formula I, is reacted with an aliphatic or aromatic peroxocarboxylic acid, preferably in the presence of from 0 to 15 moles of an alkali metal hydroxide, alkaline earth metal hydroxide, alkali meteal carbonate or alkaline earth metal carbonate in such a way that the reaction temperature is from -5.degree. C. to 60.degree.C.The reaction can be carried out in water as a solvent or in a 2-phase system consisting of water and an inert organic solvent which is poorly miscible with water, in the presence or absence of a suitable phase transfer catalyst. The peroxocarboxylic acid can be prepared in the reaction mixture before the reaction from H.sub.2 O.sub.2 and an acyl halide or a carboxylic anhydride or can be used in the form of an alkali metal salt or alkaline earth metal salt.