JPH0224823B
Azole derivs. of formula (I), their acid addn. salts and metal salt complexes are new. R is alkyl or opt. substd. cycloalkyl or phenyl. X is nitrogen or CH. Y is OCH2, CH2CH2 or CH=CH. Z is halo, alkyl (opt. substd. by halo), cycloalkyl, alkoxy or alkylthio (both opt. substd. by halo) or opt. substd...
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| creator | KARURU HAINTSU BYUTSUHIERU KURAUSU RYURUSEN UIRUHERUMU BURANDESU GURAHAMU HORUMUTSUDO PAURUUERUNSUTO FUROOBERUGAA |
| description | Azole derivs. of formula (I), their acid addn. salts and metal salt complexes are new. R is alkyl or opt. substd. cycloalkyl or phenyl. X is nitrogen or CH. Y is OCH2, CH2CH2 or CH=CH. Z is halo, alkyl (opt. substd. by halo), cycloalkyl, alkoxy or alkylthio (both opt. substd. by halo) or opt. substd. phenyl, phenoxy, phenylalkyl or phenylalkoxy. m is 0-3. Also new are intermediates of formula (II). (I) are useful as fungicides (esp. against true mildews such as Erysiphe species and have both preventative and systemic actions and as plant-growth regulators. Typical responses include inhibiting vegetative growth of cereals etc., increasing sugar content of beet, and protein content of soya; stimulating latex flow in rubber trees; induction of parthenocarpic fruiting; breaking apical dominance, defoliation, acceleration of ripening; improving resistance to adverse climatic conditions etc. They are more effective than known cpds. such as 2-chloroethylphosphonic acid. |
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R is alkyl or opt. substd. cycloalkyl or phenyl. X is nitrogen or CH. Y is OCH2, CH2CH2 or CH=CH. Z is halo, alkyl (opt. substd. by halo), cycloalkyl, alkoxy or alkylthio (both opt. substd. by halo) or opt. substd. phenyl, phenoxy, phenylalkyl or phenylalkoxy. m is 0-3. Also new are intermediates of formula (II). (I) are useful as fungicides (esp. against true mildews such as Erysiphe species and have both preventative and systemic actions and as plant-growth regulators. Typical responses include inhibiting vegetative growth of cereals etc., increasing sugar content of beet, and protein content of soya; stimulating latex flow in rubber trees; induction of parthenocarpic fruiting; breaking apical dominance, defoliation, acceleration of ripening; improving resistance to adverse climatic conditions etc. They are more effective than known cpds. such as 2-chloroethylphosphonic acid.</description><language>eng</language><subject>AGRICULTURE ; ANIMAL HUSBANDRY ; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES ; CHEMISTRY ; FISHING ; FORESTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HUNTING ; METALLURGY ; ORGANIC CHEMISTRY ; PEST REPELLANTS OR ATTRACTANTS ; PLANT GROWTH REGULATORS ; PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF ; TRAPPING</subject><creationdate>1990</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19900530&DB=EPODOC&CC=JP&NR=H0224823B2$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19900530&DB=EPODOC&CC=JP&NR=H0224823B2$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KARURU HAINTSU BYUTSUHIERU</creatorcontrib><creatorcontrib>KURAUSU RYURUSEN</creatorcontrib><creatorcontrib>UIRUHERUMU BURANDESU</creatorcontrib><creatorcontrib>GURAHAMU HORUMUTSUDO</creatorcontrib><creatorcontrib>PAURUUERUNSUTO FUROOBERUGAA</creatorcontrib><title>JPH0224823B</title><description>Azole derivs. of formula (I), their acid addn. salts and metal salt complexes are new. 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R is alkyl or opt. substd. cycloalkyl or phenyl. X is nitrogen or CH. Y is OCH2, CH2CH2 or CH=CH. Z is halo, alkyl (opt. substd. by halo), cycloalkyl, alkoxy or alkylthio (both opt. substd. by halo) or opt. substd. phenyl, phenoxy, phenylalkyl or phenylalkoxy. m is 0-3. Also new are intermediates of formula (II). (I) are useful as fungicides (esp. against true mildews such as Erysiphe species and have both preventative and systemic actions and as plant-growth regulators. Typical responses include inhibiting vegetative growth of cereals etc., increasing sugar content of beet, and protein content of soya; stimulating latex flow in rubber trees; induction of parthenocarpic fruiting; breaking apical dominance, defoliation, acceleration of ripening; improving resistance to adverse climatic conditions etc. They are more effective than known cpds. such as 2-chloroethylphosphonic acid.</abstract><oa>free_for_read</oa></addata></record> |
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| subjects | AGRICULTURE ANIMAL HUSBANDRY BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES CHEMISTRY FISHING FORESTRY HETEROCYCLIC COMPOUNDS HUMAN NECESSITIES HUNTING METALLURGY ORGANIC CHEMISTRY PEST REPELLANTS OR ATTRACTANTS PLANT GROWTH REGULATORS PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF TRAPPING |
| title | JPH0224823B |
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