JP6514229B2 - 植物病害防除組成物及びそれを施用する植物病害の防除方法 - Google Patents
植物病害防除組成物及びそれを施用する植物病害の防除方法 Download PDFInfo
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Classifications
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
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- A—HUMAN NECESSITIES
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- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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Description
(a)一般式(I):
[式中、R1及びR2は、同一若しくは異なっていてもよく、
メチル基、エチル基、プロピル基、トリフルオロメチル基、トリフルオロエチル基、フェニル基、フルオロフェニル基又はクロロフェニル基であり、
R3及びR4は、同一若しくは異なっていてもよく、
水素原子、フッ素原子又はメチル基であり、
Xは、フッ素原子、塩素原子、臭素原子、メチル基、エチニル基、フリル基、チエニル基、シアノ基、メトキシエタンイミドイル基、エトキシエタンイミドイル基又はフェノキシエタンイミドイル基であり、nが、0、1又は2であり、
Yは、フッ素原子又はメチル基であり、mが、0又は1である]
で表される少なくとも1種のキノリン化合物又はその塩(グループa)及び
(b−1)フルキサピロキサド(Fluxapyroxad)、
(b−2)ベンゾビンジフルピル(Benzovindiflupyr)、
(b−3)式(II)の化合物
(b−4)ビキサフェン(Bixafen)、
(b−5)ペンフルフェン(Penflufen)
(b−6)セダキサン(Sedaxane)、
(b−7)イソピラザム(Isopyrazam)、
(b−8)式(III)の化合物
(b−9)式(IV)の化合物
からなるピラゾールカルボキサミド類;
(b−10)エノキサストロビン(Enoxastrobin)、
(b−11)ピラオキシストロビン(Pyraoxystrobin)、
(b−12)クモキシストロビン(Coumoxystrobin)、
(b−13)クメトキシストロビン(Coumethoxystrobin)、
(b−14)フルフェノキシストロビン(Flufenoxystrobin)、
(b−15)ピリミノストロビン(Pyriminostrobin)及び
(b−16)ピコキシストロビン(Picoxystrobin)
からなるメトキシアクリレート類;
(b−17)ピラメトストロビン(Pyrametostrobin)、
(b−18)トリクロピリカルブ(Triclopyricarb)及び
(b−19)ピラクロストロビン(Pyraclostrobin)
からなるメトキシカーバメート類;
(b−20)イマザリル(Imazalil)、
(b−21)プロクロラズ(Prochloraz)、
(b−22)テトラコナゾール(Tetraconazole)、
(b−23)プロチオコナゾール(Prothioconazole)、
(b−24)エポキシコナゾール(Epoxiconazole)、
(b−25)イプコナゾール(Ipconazole)、
(b−26)メトコナゾール(Metconazole)、
(b−27)プロピコナゾール(Propiconazole)、
(b−28)シプロコナゾール(Cyproconazole)、
(b−29)ジフェノコナゾール(Difenoconazole)、
(b−30)フルキンコナゾール(Fluquinconazole)、
(b−31)フルシラゾール(Flusilazole)、
(b−32)ペンコナゾール(Penconazole)、
(b−33)トリアジメノール(Triadimenol)、
(b−34)フルトリアフォル(Flutriafol)、
(b−35)ミクロブタニル(Myclobutanil)、
(b−36)式(V)の化合物
式中、Rb7は水素原子、アルキル基、アリル基、ベンジル基、アミノ基、シアノ基であるか、又は結合であって硫黄原子とトリアゾール環との間に二重結合を形成し
で示す環を形成することを表し、
Rb8は水素原子、又はフッ素原子を表す、
(b−37)式(VI)の化合物
式中、破線部分は、存在しないか、又は結合を表し、
Rb9は水素原子、アルキル基、アリル基、ベンジル基、シアノ基を表す、及び
(b−38)式(VII)の化合物
式中、Rb10はハロゲン原子を表し、
Rb11は、窒素原子またはメチン基を表す、
からなるアゾール系化合物;
(b−39)ゾキサミド(Zoxamide)、
(b−40)フルオピコリド(Fluopicolide)、
(b−41)カルボキシン(Carboxin)、
(b−42)チフルザミド(Thifluzamide)、
(b−43)フルオピラム(Fluopyram)、
(b−44)マンジプロパミド(Mandipropamid)、
(b−45)チアジニル(Tiadinil)、
(b−46)イソチアニル(Isotianil)、
(b−47)イソフェタミド(Isofetamid)、
(b−48)バリフェナレート(Valifenalate)、
(b−49)ピラジフルミド(pyraziflumid)
(b−50)イプロバリカルブ(Iprovalicarb)
からなるアミド系化合物;
(b−51)フルオキサストロビン(Fluoxastrobin)、
(b−52)ジモキシストロビン(Dimoxystrobin)、
(b−53)オリサストロビン(Orysastrobin)、
(b−54)メトミノストロビン(Metominostrobin)、
(b−55)トリフロキシストロビン(Trifloxystrobin)、
(b−56)マンデストロビン(Mandestrobin)及び
(b−57)フェナミンストロビン(Fenaminstrobin)
からなるストロビルリン系化合物;
(b−58)ベノミル(Benomyl)、
(b−59)カルベンダジム(Carbendazim)及び
(b−60)チアベンダゾール(Thiabendazole)
からなるベンズイミダゾール系化合物;
(b−61)シプロジニル(Cyprodinil)及び
(b−62)ピリメタニル(Pyrimethanil)
からなるピリミジン系化合物;
(b−63)キノキシフェン(Quinoxyfen)及び
b−64)テブフロキン(Tebufloquin)
からなるキノリン系化合物;
(b−65)フェンプロピモルフ(Fenpropimorph)及び
(b−66)トリデモルフ(Tridemorph)
からなるモルホリン系化合物;
(b−67)メチラム(Metiram)、
(b−68)チウラム(Thiuram)、
(b−69)プロピネブ(Propineb)、
(b−70)ホルペット(Folpet)、
(b−71)イソプロチオラン(Isoprothiolane)、
(b−72)アシベンゾラル−S−メチル(Acibenzolar−S−methyl)
(b−73)プロベナゾール(Probenazole)及び
(b−74)キノメチオネート(Chinomethionat)
からなる有機硫黄系化合物;
(b−75)ベナラキシル−M(Benalaxyl−M)、
(b−76)ペンシクロン(Pencycuron)及び
(b−77)フルチアニル(Flutianil)
からなるアニリド系化合物;
(b−78)ピカルブトラゾックス(Picarbutrazox)及び
(b−79)式(VIII)の化合物
式中、Rb12は
からなるアミノピリジン系化合物;
(b−80)
及び
(b−81)ジチアノン(Dithianon)
からなるジチイン系化合物;
(b−82)メトラフェノン(Metrafenone)及び
(b−83)ピリオフェノン(Pyriofenone)
からなるフェニルケトン系化合物;
(b−84)オキサチアピプロリン(Oxathiapiprolin);
(b−85)式(XI)の化合物
式中、Rb1は塩素原子、臭素原子、シアノ基、メチル基又はメトキシ基を表し、
Rb2はフッ素原子又は水素原子を表し、
Rb3はハロゲン原子を表し、
Rb4はハロゲン原子、メトキシ基又は水素原子を表し、
Zは、N又はC−Fを表す、
(b−86)式(XII)の化合物
式中、Rb5はメチル基又はフッ素を表す;
(b−87)式(XIII)の化合物
式中、Rb6は−CH2OC(O)CH(CH3)2、−C(O)CH3、−CH2OC(O)CH3、−C(O)OCH2CH(CH3)2、または
(b−88)式(XIV)の化合物
(b−89)式(XV)の化合物
式中、Rb13は塩素原子又はフッ素原子を表し、
Rb14は塩素原子又は水素原子を表し、
Rb15は塩素原子又は臭素原子を表す;
(b−90)式(XVI)の化合物
式中、Rb16はフッ素原子又はメチル基を表す、
からなるその他の殺菌剤(i);
(b−91)式(XVII)の化合物
(b−92)式(XVIII)の化合物
(b−93)D−タガトース(D−tagatose)、
(b−94)式(XIX)の化合物
式中、Rb17は水素原子又はフッ素原子を表す、
からなるその他の殺菌剤(ii);
(b−95)アメトクトラジン(Ametoctradin)、
(b−96)硫黄(Sulfur)、
(b−97)アミスルブロム(Amisulbrom)、
(b−98)ピリベンカルブ(Pyribencarb)、
(b−99)フェンピラザミン(Fenpyrazamine)、
(b−100)プロキナジド(Proquinazid)、
(b−101)スピロキサミン(Spiroxamine)、
(b−102)フェンプロピジン(Fenpropidin)、
(b−103)ピリソキサゾール(Pyrisoxazole)、
(b−104)ピロキロン(Pyroquilon)、
(b−105)亜燐酸(Phosphorous acid)及び
(b−106)ヒドロキシイソキサゾール(Hydroxyisoxazol:Hymexazol)
からなるその他の殺菌剤(iii);
から選択される1種以上の殺菌性化合物を有効成分として含有することを特徴とする植物病害防除組成物である。
なお、一般式(I)で表されるキノリン化合物において、mが0のときは、Ymは水素原子を表し、nが0のときは、Xnは水素原子を表す。
好適には、
(a−1)3−(5−フルオロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−2)3−(5−クロロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−3)3−(5−ブロモ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−4)3−(5−エチニル−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−5)3−(5,6−ジフルオロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−6)3−(3−エチル−5−フルオロ−3−プロピル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−7)3−(5−フルオロ−3−メチル−3−プロピル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−8)3−(3−メチル−3−トリフルオロメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン
(a−9)3−[3−メチル−3−(2,2,2−トリフルオロエチル)−3,4−ジヒドロイソキノリン−1−イル]キノリン、
(a−10)3−[3−メチル−3−フェニル−3,4−ジヒドロイソキノリン−1−イル]キノリン、
(a−11)3−[3−メチル−3−(4−フルオロフェニル)−3,4−ジヒドロイソキノリン−1−イル]キノリン、
(a−12)3−[3−メチル−3−(4−クロロフェニル)−3,4−ジヒドロイソキノリン−1−イル]キノリン、
(a−13)3−(3,3,4,4−テトラメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−14)3−(5−フルオロ−3,3,4,4−テトラメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−15)3−(5−フルオロ−3,3,4,4−テトラメチル−3,4−ジヒドロイソキノリン−1−イル)−6−フルオロキノリン、
(a−16)3−(5−フルオロ−3,3,4,4−テトラメチル−3,4−ジヒドロイソキノリン−1−イル)−8−フルオロキノリン、
(a−17)3−(5−フルオロ−3,3,4,4−テトラメチル−3,4−ジヒドロイソキノリン−1−イル)−8−メチルキノリン、
(a−18)3−(4,4−ジフルオロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−19)3−(4,5−ジフルオロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン又は
(a−20)3−(4,4,5−トリフルオロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン
又はその塩である。
(a−14)3−(5−フルオロ−3,3,4,4−テトラメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−18)3−(4,4−ジフルオロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−20)3−(4,4,5−トリフルオロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、及び
その塩
からなる群より選択される。
(b−1)フルキサピロキサド(Fluxapyroxad)、
(b−2)ベンゾビンジフルピル(Benzovindiflupyr)、
(b−3)式(II)の化合物
(b−4)ビキサフェン(Bixafen)
(b−5)ペンフルフェン(Penflufen)
(b−6)セダキサン(Sedaxane)、
(b−7)イソピラザム(Isopyrazam)、
(b−8)式(III)の化合物
及び
(b−9)式(IV)の化合物
からなるピラゾールカルボキサミド類;
(b−16)ピコキシストロビン(Picoxystrobin)
からなるメトキシアクリレート類;
(b−19)ピラクロストロビン(Pyraclostrobin)
からなるメトキシカーバメート類;
(b−20)イマザリル(Imazalil)、
(b−21)プロクロラズ(Prochloraz)、
(b−22)テトラコナゾール(Tetraconazole)、
(b−23)プロチオコナゾール(Prothioconazole)、
(b−24)エポキシコナゾール(Epoxiconazole)、
(b−25)イプコナゾール(Ipconazole)、
(b−26)メトコナゾール(Metconazole)、
(b−27)プロピコナゾール(Propiconazole)、
(b−28)シプロコナゾール(Cyproconazole)、
(b−29)ジフェノコナゾール(Difenoconazole)、
(b−30)フルキンコナゾール(Fluquinconazole)、
(b−31)フルシラゾール(Flusilazole)、
(b−32)ペンコナゾール(Penconazole)、
(b−33)トリアジメノール(Triadimenol)、
(b−34)フルトリアフォル(Flutriafol)、
(b−35)ミクロブタニル(Myclobutanil)、
(b−36)式(V)の化合物
式中、Rb7は水素原子、アルキル基、アリル基、ベンジル基、シアノ基であるか、又は結合であって硫黄原子とトリアゾール環との間に二重結合を形成し
で示す環を形成することを表し、
Rb8は水素原子、又はフッ素原子を表す、
(b−38)式(VII)の化合物
式中、Rb10はハロゲン原子を表し、
Rb11は、窒素原子またはメチン基を表す、
からなるアゾール系化合物;
(b−39)ゾキサミド(Zoxamide)、
(b−40)フルオピコリド(Fluopicolide)、
(b−41)カルボキシン(Carboxin)、
(b−42)チフルザミド(Thifluzamide)、
(b−43)フルオピラム(Fluopyram)、
(b−44)マンジプロパミド(Mandipropamid)、
(b−45)チアジニル(Tiadinil)、
(b−46)イソチアニル(Isotianil)、
(b−47)イソフェタミド(Isofetamid)、
(b−49)ピラジフルミド(pyraziflumid)
及び
(b−50)イプロバリカルブ(Iprovalicarb)
からなるアミド系化合物;
(b−51)フルオキサストロビン(Fluoxastrobin)、
(b−52)ジモキシストロビン(Dimoxystrobin)、
(b−53)オリサストロビン(Orysastrobin)、
(b−54)メトミノストロビン(Metominostrobin)及び
(b−55)トリフロキシストロビン(Trifloxystrobin)
からなるストロビルリン系化合物;
(b−58)ベノミル(Benomyl)、
(b−59)カルベンダジム(Carbendazim)及び
(b−60)チアベンダゾール(Thiabendazole)
からなるベンズイミダゾール系化合物;
(b−61)シプロジニル(Cyprodinil)及び
(b−62)ピリメタニル(Pyrimethanil)
からなるピリミジン系化合物;
(b−63)キノキシフェン(Quinoxyfen)及び
(b−64)テブフロキン(Tebufloquin)
からなるキノリン系化合物;
(b−65)フェンプロピモルフ(Fenpropimorph)及び
(b−66)トリデモルフ(Tridemorph)
からなるモルホリン系化合物;
(b−67)メチラム(Metiram)、
(b−68)チウラム(Thiuram)、
(b−69)プロピネブ(Propineb)、
(b−70)ホルペット(Folpet)、
(b−71)イソプロチオラン(Isoprothiolane)、
(b−72)アシベンゾラル−S−メチル(Acibenzolar−S−methyl)
(b−73)プロベナゾール(Probenazole)及び
(b−74)キノメチオネート(Chinomethionat)
からなる有機硫黄系化合物;
(b−75)ベナラキシル−M(Benalaxyl−M)、
(b−76)ペンシクロン(Pencycuron)及び
(b−77)フルチアニル(Flutianil)
からなるアニリド系化合物;
(b−78)ピカルブトラゾクス(Picarbutrazox)
からなるアミノピリジン系化合物;
(b−81)ジチアノン(Dithianon)
からなるジチイン系化合物;
(b−82)メトラフェノン(Metrafenone)及び
(b−83)ピリオフェノン(Pyriofenone)
からなるフェニルケトン系化合物;
(b−84)オキサチアピプロリン(Oxathiapiprolin);
(b−85)式(XI)の化合物
式中、Rb1は塩素原子、臭素原子、シアノ基、メチル基又はメトキシ基を表し、
Rb2はフッ素原子又は水素原子を表し、
Rb3はハロゲン原子を表し、
Rb4はハロゲン原子、メトキシ基又は水素原子を表し、
Zは、N又はC−Fを表す、
(b−88)式(XIV)の化合物
(b−89)式(XV)の化合物
式中、Rb13は塩素原子又はフッ素原子を表し、
Rb14は塩素原子又は水素原子を表し、
Rb15は塩素原子又は臭素原子を表す、
からなるその他の殺菌剤(i);
(b−91)式(XVII)の化合物
(b−92)式(XVIII)の化合物
(b−93)D−タガトース(D−tagatose)、及び
(b−94)式(XIX)の化合物
式中、Rb17は水素原子又はフッ素原子を表す、
からなるその他の殺菌剤(ii);
(b−95)アメトクトラジン(Ametoctradin)、
(b−96)硫黄(Sulfur)、
(b−97)アミスルブロム(Amisulbrom)、
(b−98)ピリベンカルブ(Pyribencarb)、
(b−99)フェンピラザミン(Fenpyrazamine)、
(b−100)プロキナジド(Proquinazid)、
(b−101)スピロキサミン(Spiroxamine)、
(b−102)フェンプロピジン(Fenpropidin)、
(b−103)ピリソキサゾール(Pyrisoxazole)、
(b−104)ピロキロン(Pyroquilon)、
(b−105)亜燐酸(Phosphorous acid)及び
(b-106)ヒドロキシイソキサゾール(Hydroxyisoxazol:Hymexazol)
からなるその他の殺菌剤(iii);
から選択され、さらに好適には、
(b−2)ベンゾビンジフルピル(Benzovindiflupyr)及び
(b−3)式(II)の化合物
(b−8)式(III)の化合物
(b−9)式(IV)の化合物
からなるピラゾールカルボキサミド類;
(b−36)式(V)の化合物
式中、Rb7は水素原子、アルキル基、アリル基、ベンジル基、シアノ基であるか、又は結合であって硫黄原子とトリアゾール環との間に二重結合を形成し
で示す環を形成することを表し、
Rb8は水素原子、又はフッ素原子を表す、
(b−38)式(VII)の化合物
式中、Rb10はハロゲン原子を表し、
Rb11は、窒素原子またはメチン基を表す、
からなるアゾール系化合物;
(b−47)イソフェタミド(Isofetamid)及び
(b−49)ピラジフルミド(pyraziflumid)
からなるアミド系化合物;
(b−78)ピカルブトラゾクス(Picarbutrazox)
からなるアミノピリジン系化合物;
(b−84)オキサチアピプロリン(Oxathiapiprolin);
(b−85)式(XI)の化合物
式中、Rb1は塩素原子、臭素原子、シアノ基、メチル基又はメトキシ基を表し、
Rb2はフッ素原子又は水素原子を表し、
Rb3はハロゲン原子を表し、
Rb4はハロゲン原子、メトキシ基又は水素原子を表し、
Zは、N又はC−Fを表す、
(b−88)式(XIV)の化合物
(b−89)式(XV)の化合物
式中、Rb13は塩素原子又はフッ素原子を表し、
Rb14は塩素原子又は水素原子を表し、
Rb15は塩素原子又は臭素原子を表す、
からなるその他の殺菌剤(i);
(b−91)式(XVII)の化合物
(b−92)式(XVIII)の化合物
(b−93)D−タガトース(D−tagatose)、
(b−94)式(XIX)の化合物
式中、Rb17は水素原子又はフッ素原子を表す、
からなるその他の殺菌剤(ii);
から選択され、さらになお好適には、
(b−2)ベンゾビンジフルピル(Benzovindiflupyr)及び
(b−3)式(II)の化合物
からなるピラゾールカルボキサミド類;
(b−10)エノキサストロビン(Enoxastrobin)、
(b−11)ピラオキシストロビン(Pyraoxystrobin)、
(b−12)クモキシストロビン(Coumoxystrobin)、
(b−13)クメトキシストロビン(Coumethoxystrobin)、
(b−14)フルフェノキシストロビン(Flufenoxystrobin)及び
(b−15)ピリミノストロビン(Pyriminostrobin)
からなるメトキシアクリレート類;
(b−17)ピラメトストロビン(Pyrametostrobin)及び
(b−18)トリクロピリカルブ(Triclopyricarb)
からなるメトキシカーバメート類;
(b−84)オキサチアピプロリン(Oxathiapiprolin);
(b−56)マンデストロビン(Mandestrobin);
(b−47)イソフェタミド(Isofetamid);
(b−78)ピカルブトラゾックス(Picarbutrazox);
(b−57)フェナミンストロビン(Fenaminstrobin);
(b−48)バリフェナレート(Valifenalate);
(b−49)ピラジフルミド(pyraziflumid)
(b−85)式(XI’)の化合物
式中、Rb1は塩素原子、臭素原子、シアノ基、メチル基又はメトキシ基を表し、
Rb2はフッ素原子又は水素原子を表し、
Rb3はハロゲン原子を表し、
Rb4はハロゲン原子、メトキシ基又は水素原子を表す;
(b−86)式(XII)の化合物
式中、Rb5はメチル基又はフッ素原子を表す;
(b−87)式(XIII)の化合物
式中、Rb6は−CH2OC(O)CH(CH3)2、−C(O)CH3、−CH2OC(O)CH3、−C(O)OCH2CH(CH3)2、または
(b−88)式(XIV)の化合物
(b−89)式(XV)−1の化合物
(b−80)
及び
(b−90)式(XVI)−1の化合物
(b−36)式(V)の化合物
式中、Rb7は水素原子、アルキル基、アミノ基、シアノ基を表し、
Rb8は水素原子、又はフッ素原子を表す、
(b−37’)式(VI’)の化合物
式中、破線部分は、存在しないか、又は結合を表し、
Rb9は水素原子、アルキル基、アミノ基、シアノ基を表す;
(b−38)式(VII)の化合物
式中、Rb10はハロゲン原子を表し、
Rb11は、窒素原子またはメチン基を表す、及び
(b−79)式(VIII)の化合物
式中、Rb12は
から選択され、より一層好適には、
(b−2)ベンゾビンジフルピル(Benzovindiflupyr)、及び
(b−3)式(II)の化合物
からなるピラゾールカルボキサミド類;
(b−47)イソフェタミド(Isofetamid);
(b−78)ピカルブトラゾックス(Picarbutrazox);
(b−49)ピラジフルミド(pyraziflumid)
(b−85)式(XI’)の化合物
式中、Rb1は塩素原子、臭素原子、シアノ基、メチル基又はメトキシ基を表し、
Rb2はフッ素原子又は水素原子を表し、
Rb3はハロゲン原子を表し、
Rb4はハロゲン原子、メトキシ基又は水素原子を表す、
(b−88)式(XIV)の化合物
(b−89)式(XV)−1の化合物
(b−36)式(V)の化合物
式中、Rb7は水素原子、アルキル基、アミノ基、シアノ基を表し、
Rb8は水素原子、又はフッ素原子を表す、
(b−37’)式(VI’)の化合物
式中、破線部分は、存在しないか、又は結合を表し、
Rb9は水素原子、アルキル基、アミノ基、シアノ基を表す;
(b−38)式(VII)の化合物
式中、Rb10はハロゲン原子を表し、
Rb11は、窒素原子またはメチン基を表す、及び
(b−79)式(VIII)の化合物
式中、Rb12は
から選択され、最も好適には、
(b−2)ベンゾビンジフルピル(Benzovindiflupyr)、及び
(b−3)式(II)の化合物
からなるピラゾールカルボキサミド類;
(b−47)イソフェタミド(Isofetamid);
(b−78)ピカルブトラゾックス(Picarbutrazox);
(b−49)ピラジフルミド(pyraziflumid);
(b−88)式(XIV)の化合物
及び
(b−38)式(VII)の化合物
式中、Rb10はハロゲン原子を表し、
Rb11は、窒素原子またはメチン基を表す;
から選択される。
で表される(b−36)の化合物は、Rb7が結合であって硫黄原子とトリアゾール環との間に二重結合を形成して
で示す環を形成し、Rb8がフッ素原子である場合、すなわち、式:
で表される化合物であることが好ましい。
(b−4)ビキサフェン(Bixafen)
(b−19)ピラクロストロビン(Pyraclostrobin)
(b−23)プロチオコナゾール(Prothioconazole)
(b−26)メトコナゾール(Metconazole)
(b−29)ジフェノコナゾール(Difenoconazole)
(b−33)トリアジメノール(Triadimenol)
(b−43)フルオピラム(Fluopyram)
(b−46)イソチアニル(Isotianil)
(b−52)ジモキシストロビン(Dimoxystrobin)
(b−54)メトミノストロビン(Metominostrobin)
(b−55)トリフロキシストロビン(Trifloxystrobin)
(b−62)ピリメタニル(Pyrimethanil)
(b−69)プロピネブ(Propineb)
(b−81)ジチアノン(Dithianon)
(b−101)スピロキサミン(Spiroxamine)及び
(b−105)亜燐酸(Phosphorous acid)
からなる群より選択されることが好ましい。
イネのいもち病(Pyricularia oryzae)、ごま葉枯病(Cochliobolus miyabeanus)、馬鹿苗病(Gibberella fujikuroi)、苗立枯病(Fusarium spp.、Trichoderma spp.、Rhizopus spp.、等)、稲こうじ病(Claviceps virens);ムギ類のうどんこ病(Erysiphe graminis f.sp.hordei; f.sp.tritici)、斑葉病(Pyrenophora graminea)、網斑病(Pyrenophora teres)、赤かび病(Fusarium graminearum、Fusarium culmorum、Fusarium avenaceum、Microdochium nivale)、雪腐病(Typhula incarnata、Typhula ishikariensis、Micronectriella nivalis)、眼紋病(Pseudocercosporella herpotrichoides)、株腐病(Rhizoctonia cerealis)、雲形病(Rhynchosporium secalis)、葉枯病(Septoria tritici)、ふ枯病(Leptosphaeria nodorum)、苗立枯病(Fusarium spp.、Pythium spp.、Rhizoctonia spp.、Septoria nodorum、Pyrenophora spp.)、立枯病(Gaeumannomyces graminis)、炭疽病(Colletotrichum gramaminicola)、麦角病(Claviceps purpurea)、斑点病(Cochliobolus sativus);トウモロコシの赤かび病(Fusarium graminearum等)、苗立枯病(Fusarium avenaceum、 Penicillium spp、 Pythium spp.、)、ごま葉枯病(Cochliobolus heterostrophus)、北方斑点病(Cochliobolus carbonum);ブドウのうどんこ病(Uncinula necator)、黒とう病(Elsinoe ampelina)、晩腐病(Glomerella cingulata)、黒腐病(Guignardia bidwellii)、つる割病(Phomopsis viticola)、すす点病(Zygophiala jamaicensis)、灰色かび病(Botrytis cinerea)、芽枯病(Diaporthe medusaea)、紫紋羽病(Helicobasidium mompa)、白紋羽病(Rosellinia necatrix);リンゴのうどんこ病(Podosphaera leucotricha)、黒星病(Venturia inaequalis)、斑点落葉病(Alternaria alternata(Apple pathotype))、モニリア病(Monillia mali)、腐らん病(Valsa ceratosperma)、輪紋病(Botryosphaeria berengeriana)、炭疽病(Colletotrichum acutatum)、すす点病(Zygophiala jamaicensis)、すす斑病(Gloeodes pomigena)、黒点病(Mycosphaerella pomi)、紫紋羽病(Helicobasidium mompa)、白紋羽病(Rosellinia necatrix)、胴枯病(Phomopsis mali、Diaporthe tanakae)、褐斑病(Diplocarpon mali);ナシの黒斑病(Alternaria alternata(Japanese pear pathotype))、黒星病(Venturia nashicola)、輪紋病(Physalospora piricola)、胴枯病(Diaporthe medusaea、Diaporthe eres);モモの黒星病(Cladosporium carpophilum)、フォモプシス腐敗病(Phomopsis sp.)、炭疽病(Gloeosporium laeticolor);オウトウの炭疽病(Glomerella cingulata)、幼果菌核病(Monilinia kusanoi)、灰星病(Monilinia fructicola);カキの炭疽病(Gloeosporium kaki)、落葉病(Cercospora kaki; Mycosphaerella nawae)、うどんこ病(Phyllactinia kakikora);カンキツの黒点病(Diaporthe citri)、緑かび病(Penicillium digitatum)、青かび病(Penicillium italicum)、そうか病(Elsinoe fawcettii);
成分I(グループa)としての、化合物A、B及びCのいずれか一つの化合物(10部、1部、又は0.01部)、成分II(グループb)としての、下記に記載のいずれか一つの化合物(添加量)、ネオゲンパウダー(0.5部)、カープレックス(0.5部)、ゴーセノール(0.2部)、ラヂオライト(0.8部)およびH微粉(合計100部になるように、残部として用いた)を粉砕混合して水和剤(a1)を得た。
成分I(グループa)としての、化合物A、B及びCのいずれか一つの化合物(10部、又は1部)、成分II(グループb)としての、下記に記載のいずれか一つの化合物(添加量)、プロピレングリコール(7部)、リグニンスルホン酸ナトリウム(4部)、ジオクチルスルホサクシネートナトリウム塩(2部)および水(合計100部になるように、残部として用いた)をサンドグラインダーで湿式粉砕し、フロアブル剤(b1)を得た。
成分I(グループa)としての、化合物A、B及びCのいずれか一つの化合物(10部、又は1部)、成分II(グループb)としての、下記に記載のいずれか一つの化合物(添加量)、シクロヘキサン(10部)、Tween20(界面活性剤:20部)、キシレン(合計100部になるように、残部として用いた)を均一に溶解混合し、乳剤(c1)を得た。
成分I(グループa)、または成分II(グループb)のいずれか片方の化合物のみを含有させる以外、製剤例1と同様な方法により、水和剤(a2)を得た。
成分I(グループa)、または成分II(グループb)のいずれか片方の化合物のみを含有させる以外、製剤例2と同様な方法により、フロアブル剤(b2)を得た。
成分I(グループa)、または成分II(グループb)のいずれか片方の化合物のみを含有させる以外、製剤例3と同様な方法により、乳剤(c2)を得た。
水和剤(a1)で用いられている成分II(グループb)化合物に代えて下記成分II(グループb)化合物を含有させる以外、製剤例1と同様な方法により、水和剤(a3)を得た。成分II(グループb)としての化合物(添加量)は、ジクロシメット(Diclocymet)(0.4〜50部)、カルプロパミド(Carpropamid)(0.4〜50部)、トルクロホスメチル(Tolclofos−methyl)(10〜50部)、及びオキソリニック酸(Oxolinic acid)(50部)である。
温室内にて、直径5cmのプラスチックポットに植えられたトマト(品種:大型福寿)を第2〜3葉期まで生育させた。製剤例1及び比較製剤例1に準じて調製した製剤の内、表2に示した化合物を含有する水和剤について、水で所定濃度に希釈し、2ポットあたり5mlずつ、スプレーガンにて散布した。薬液が乾いた後に、予めPDA培地上で培養した灰色かび病菌から調製した分生胞子懸濁液を、噴霧接種した。接種後、人工接種室(25℃)の湿室内にポットを入れ、2日間経過後に取り出し、防除効果を調査した。調査において、トマトの1葉当りに占める病斑面積の割合を下記発病程度の指標に従って決定した。また、各処理区の平均発病程度から下記の計算式により防除価を算出した。散布試験結果およびコルビーの式による理論値を表2に示す。
指標 発病程度
0 病斑無し
0.5 病斑面積率1〜2%程度
1 病斑面積率5%未満
2 病斑面積率25%未満
3 病斑面積率50%未満
4 病斑面積率75%未満
5 病斑面積率95%未満
6 病斑面積率95%以上または枯死
なお、各処理区および無処理区の平均値を発病程度とした。
防除価=(1−処理区の発病小葉率/無処理区の発病小葉率)×100
なお、相乗効果は、コルビー(Colby)の式により判定した。コルビーの式は、 X=P+Q−P×Q/100であり、ここで、Xは、防除価の理論値であり、Pはある薬剤を単独で散布した場合の防除価であり、Qは、併用する薬剤を単独で散布した場合の防除価である。実際に測定された効果が、上記のコルビー式で計算される効果X(理論値)よりも大きい場合は、2種の有効成分の組み合わせの作用は相加的な効果を越えていること、すなわち相乗効果が存在することを意味する。
表2−10に示した化合物を含有する比較製剤例4に準じて調製した水和剤をトマト葉に対し散布し、灰色かび病菌から調製した分生胞子懸濁液を噴霧接種し、そして防除効果を試験例1と同様の方法で調査した。結果およびコルビーの式による理論値を表2−10に示す。
温室内にて、直径5cmのプラスチックポットに植えられたイネ(品種:幸風)を3〜4葉期まで生育させた。試験例1と同様に、表3に示した化合物を含有する水和剤について散布を行い、薬液が乾いた後に、予めオートミール培地上で培養したいもち病菌から調製した分生胞子懸濁液を噴霧接種した。接種した後、人工接種室(20〜23℃)の湿室内にポットを入れ、翌日に取り出し温室へ移動した。接種7日経過後に、防除効果を調査した。調査において、イネ1ポット当りに占める病斑数を下記発病程度の指標に従って決定し、防除価及びコルビーの式による理論値も試験例1と同様に算出した。その結果を表3−1〜表3−3に示す。
0 病斑無し
0.5 病斑数1〜2個
1 病斑数3〜5個
2 病斑数6〜10個
3 病斑数11〜20個
4 病斑数21〜30個
5 病斑数31〜40個
6 病斑数41個以上または枯死
表3−5に示した化合物を含有する比較製剤例4に準じて調製した水和剤をイネ葉に対し散布し、いもち病菌から調製した分生胞子懸濁液を噴霧接種し、そして防除効果を試験例2同様の方法で調査した。その結果及びコルビーの式による理論値を表3−5に示す。
温室内にて、直径5cmのプラスチックポットに植えられた大麦(品種:赤神力)を2〜4葉期まで生育させた。試験例1と同様に、表4に示した化合物を含有する水和剤について散布を行い、薬液が乾いた後に、オオムギうどんこ病菌の胞子を葉面上に接種した。接種した後、恒温室(20〜25℃)に移動し、接種8日経過後に、防除効果を調査した。調査において、大麦1ポット当りに占める病斑面積の割合を下記発病程度の指標に従って決定し、防除価およびコルビーの式による理論値も試験例1と同様に算出した。その結果を表4に示す。
指標 発病程度
0 病斑無し
0.5 病斑面積率1〜2%程度
1 病斑面積率5%未満
2 病斑面積率25%未満
3 病斑面積率50%未満
4 病斑面積率75%未満
5 病斑面積率75%以上
温室内にて、直径5cmのプラスチックポットに植えられた小麦(品種:農林61号)を2〜4葉期まで生育させた。試験例1と同様に、表5に示した化合物を含有する水和剤について散布を行い、薬液が乾いた後に、コムギ赤さび病菌の胞子懸濁液を葉面上に接種した。接種した後、人工接種室(20〜23℃)の湿室内にポットを入れ、翌日に取り出し温室へ移動した。接種8日経過後に、防除効果を調査した。調査において、小麦5葉当りに占める病斑数を下記発病程度の指標に従って決定し、防除価及びコルビーの式による理論値も試験例1と同様に算出した。その結果を表5に示す。
0 病斑無し
0.5 病斑数1〜2個
1 病斑数3〜5個
2 病斑数6〜20個
3 病斑数21〜50個
4 病斑数51〜80個
5 病斑数81〜100個
6 病斑数101個以上
温室内にて、直径5cmのプラスチックポットに植えられたトマト(品種:大型福寿)を第2〜3葉期まで生育させた。試験例1と同様に、表6に示した化合物を含有する水和剤について散布を行い、薬液が乾いた後に、トマト疫病菌(遊走子+遊走子嚢)懸濁液を、噴霧接種した。接種した後、人工接種室(20〜22℃)の湿室内にポットを入れ、翌日に温室へ移動し、接種5日後に、防除効果を調査した。トマト1葉当りに占める病斑面積の割合を試験例1と同様の指標に従って決定し、防除価およびコルビーの式による理論値も同様に算出した。その結果を表6−1〜表6−2に示す。
温室内にて、直径5cmのプラスチックポットに植えられたキュウリ(品種:相模半白)を3〜5葉期まで生育させた。試験例1と同様に散布を行い、散布3日後に、キュウリうどんこ病菌の胞子懸濁液を葉面上に接種した。接種した後、恒温温室(20〜25℃)に移動し、接種7日経過後に、防除効果を調査した。調査において、キュウリ1葉当りに占める病斑面積の割合を試験例1と同様の指標に従って決定し、防除価およびコルビーの式による理論値も同様に算出した。その結果を表7−1〜表7−8に示す。
表7−9に示した化合物を含有する比較製剤例4に準じて調製した水和剤をキュウリ葉に対し散布し、うどんこ病菌から調製した分生胞子懸濁液を噴霧接種し、そして防除効果を試験例6と同様の方法で調査した。その結果及びコルビーの式による理論値を表7−9に示す。
温室内にて、直径5cmのプラスチックポットに植えられたキュウリ(品種:相模半白)を3〜5葉期まで生育させた。試験例1と同様に散布を行い、薬液が乾いた後に、温室へ移動した。散布3日後に、キュウリべと病菌(遊走子嚢)懸濁液を接種した。接種した後、人工接種室(20〜25℃)の湿室内にポットを入れ、翌日に温室へ移動し、接種7日後に、防除効果を調査した。キュウリ1葉当りに占める病斑面積の割合を試験例1と同様の指標に従って決定し、防除価およびコルビーの式による理論値も同様に算出した。その結果を表8に示す。
Claims (3)
- (a)(a−14) 3−(5−フルオロ−3,3,4,4−テトラメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、
(a−18) 3−(4,4−ジフルオロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン、及び
(a−20) 3−(4,4,5−トリフルオロ−3,3−ジメチル−3,4−ジヒドロイソキノリン−1−イル)キノリン
からなる群より選択される少なくとも1種のキノリン化合物又はその塩(グループa)、及び
下記(グループb):
(b−1)フルキサピロキサド(Fluxapyroxad)、
(b−2)ベンゾビンジフルピル(Benzovindiflupyr)、
(b−3)式(II)の化合物
及び
(b−9)式(IV)の化合物
からなるピラゾールカルボキサミド類;
(b−36)式(V)の化合物
式中、Rb7は水素原子、アルキル基、アリル基、ベンジル基、アミノ基、シアノ基であるか、又は結合であって硫黄原子とトリアゾール環との間に二重結合を形成し
で示す環を形成することを表し、
Rb8は水素原子、又はフッ素原子を表す、及び
(b−38)式(VII)の化合物
式中、Rb10はハロゲン原子を表し、
Rb11は、窒素原子またはメチン基を表す、
からなるアゾール系化合物;
(b−47)イソフェタミド(Isofetamid)及び
(b−49)ピラジフルミド(pyraziflumid)
からなるアミド系化合物;
(b−78)ピカルブトラゾクス(Picarbutrazox)
からなるアミノピリジン系化合物;
(b−84)オキサチアピプロリン(Oxathiapiprolin);
(b−85)式(XI)の化合物
式中、Rb1は塩素原子、臭素原子、シアノ基、メチル基又はメトキシ基を表し、
Rb2はフッ素原子又は水素原子を表し、
Rb3はハロゲン原子を表し、
Rb4はハロゲン原子、メトキシ基又は水素原子を表し、
Zは、N又はC−Fを表す;
(b−88)式(XIV)の化合物
及び
(b−89)式(XV)の化合物
式中、Rb13は塩素原子又はフッ素原子を表し、
Rb14は塩素原子又は水素原子を表し、
Rb15は塩素原子又は臭素原子を表す、
からなるその他の殺菌剤(i);
(b−91)式(XVII)の化合物
(b−92)式(XVIII)の化合物
(b−93)D−タガトース(D−tagatose);
(b−94)式(XIX)の化合物
式中、Rb17は水素原子又はフッ素原子を表す、
からなるその他の殺菌剤(ii);
から選択される1種以上の殺菌性化合物を有効成分として含有することを特徴とする植物病害防除組成物。 - 請求項1に記載の植物病害防除組成物を施用して、植物病害を防除する防除方法。
- 植物病害を防除するための方法であって、請求項1に記載の、グループaのキノリン化合物を有効成分として含有する植物病害防除組成物及び請求項1に記載の、グループbの殺菌性化合物を有効成分として含有する植物病害防除組成物を同時に施用するか、または請求項1に記載の、グループaの化合物を有効成分として含有する植物病害防除組成物または請求項1に記載の、グループbの殺菌性化合物を有効成分として含有する植物病害防除組成物のいずれか一方を施用した後に、もう一方の前記組成物を施用することによる方法。
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Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016060230A1 (ja) * | 2014-10-16 | 2016-04-21 | 日本農薬株式会社 | 農園芸用殺菌剤及びその使用方法 |
EP3214937B1 (en) | 2014-11-07 | 2024-07-03 | Basf Se | Pesticidal mixtures |
EP3360415B1 (en) * | 2015-10-09 | 2020-07-22 | Nippon Soda Co., Ltd. | Fungicide composition for agricultural and horticultural use |
US20190045784A1 (en) * | 2016-02-26 | 2019-02-14 | Basf Se | Fungicidal mixtures comprising fluxapyroxad |
WO2017154905A1 (ja) * | 2016-03-07 | 2017-09-14 | 石原産業株式会社 | イソフェタミドの植物病害防除効果の増強方法及び植物病害の防除方法 |
EP3429357A1 (en) | 2016-03-16 | 2019-01-23 | Basf Se | Use of tetrazolinones for combating resistant phytopathogenic fungi on cereals |
BR112018068705B1 (pt) | 2016-03-16 | 2022-09-06 | Basf Se | Método para controlar fungos fitopatogênicos |
WO2017157920A1 (en) | 2016-03-16 | 2017-09-21 | Basf Se | Use of tetrazolinones for combating resistant phytopathogenic fungi on fruits |
WO2018054721A1 (en) * | 2016-09-26 | 2018-03-29 | Basf Se | Pyridine compounds for controlling phytopathogenic harmful fungi |
WO2018054711A1 (en) * | 2016-09-26 | 2018-03-29 | Basf Se | Pyridine compounds for controlling phytopathogenic harmful fungi |
EP3518675B1 (en) * | 2016-09-28 | 2020-08-19 | Syngenta Participations AG | Fungicidal compositions |
US11974572B2 (en) | 2017-03-31 | 2024-05-07 | Sygenta Participations Ag | Fungicidal compositions |
JP2021004176A (ja) | 2017-09-06 | 2021-01-14 | 石原産業株式会社 | 殺菌剤組成物及び作物の病害防除方法 |
KR102004213B1 (ko) | 2017-09-19 | 2019-08-02 | 전남대학교산학협력단 | 아시벤졸라-에스-메틸을 유효성분으로 함유하는 소나무재선충병 방제용 조성물 및 이를 이용한 소나무재선충 방제 방법 |
AU2019268861B2 (en) * | 2018-05-16 | 2021-10-21 | Nippon Soda Co., Ltd. | Safener |
CN110301436A (zh) * | 2019-08-13 | 2019-10-08 | 福建拓烯新材料科技有限公司 | 一种微胶囊剂组合物及其制备方法 |
WO2021220231A1 (en) * | 2020-05-01 | 2021-11-04 | Pi Industries Ltd. | Composition of propineb and metominostrobin |
AR128412A1 (es) * | 2022-02-04 | 2024-05-08 | Upl Corporation Ltd | Combinaciones fungicidas de al menos un fungicida de quinolina y al menos uno de anilinopirimidina |
Family Cites Families (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3575296D1 (de) | 1984-10-29 | 1990-02-15 | Sumitomo Chemical Co | Pyrazolkarboxamidabkoemmlinge, deren herstellung und diese enthaltende bakterientoetende mittel. |
DE69519087T2 (de) | 1994-04-06 | 2001-03-22 | Shionogi & Co., Ltd. | Gamma-substituierte phenylessigsäurederivate, verfahren zu ihrer herstellung und sie enthaltendes bakterizid für die landwirtschaft |
EP0936213B1 (en) | 1998-02-10 | 2003-03-26 | Dow AgroSciences LLC | Unsaturated oxime ethers and their use as fungicides and insecticides |
TR200200409T2 (tr) | 1999-08-20 | 2003-03-21 | Dow Agrosciences Llc | Mantar öldürücü heterosiklik aromatik amitler ve bileşimleri, bunları kullanma ve hazırlama yöntemleri. |
IT1318623B1 (it) | 2000-07-13 | 2003-08-27 | Isagro Ricerca Srl | Procedimento per la preparazione di derivati dipeptidici. |
US6303818B1 (en) | 2000-08-08 | 2001-10-16 | Dow Agrosciences Llc | Unsaturated oxime ethers and their use as fungicides |
PL204568B1 (pl) | 2001-08-20 | 2010-01-29 | Nippon Soda Co | Pochodna tetrazoiloksymu, pośrednie pochodne tetrahydroksyiminowe, pestycyd oraz środek zwalczający chorobę roślin, zawierające pochodną tetrazoiloksymu jako składnik aktywny |
CN1310899C (zh) | 2003-11-11 | 2007-04-18 | 沈阳化工研究院 | 具有杀虫、杀菌活性的苯并吡喃酮类化合物及制备与应用 |
PT1736471E (pt) * | 2004-01-23 | 2014-03-25 | Mitsui Chemicals Agro Inc | 3-(di-hidro(tetra-hidro)isoquinolin-1-il)quinolinas |
TWI366438B (en) | 2004-08-12 | 2012-06-21 | Ishihara Sangyo Kaisha | Fungicidal composition containing acid amide derivative |
CN100422153C (zh) | 2005-02-06 | 2008-10-01 | 沈阳化工研究院 | N-(2-取代苯基)-n-甲氧基氨基甲酸酯类化合物及其制备与应用 |
CN100427481C (zh) | 2005-05-26 | 2008-10-22 | 沈阳化工研究院 | 一种芳基醚类化合物及其制备与应用 |
JP2007001944A (ja) | 2005-06-24 | 2007-01-11 | Sankyo Agro Kk | 3,4−ジヒドロ−1,3’−ビキノリン−2−オン誘導体 |
CN100443463C (zh) | 2005-06-28 | 2008-12-17 | 沈阳化工研究院 | 取代的对三氟甲基苯醚类化合物及其制备与应用 |
WO2007011022A1 (ja) | 2005-07-22 | 2007-01-25 | Sankyo Agro Company, Limited | 3-(イソキノリン-1-イル)キノリン誘導体 |
WO2007066601A1 (ja) | 2005-12-07 | 2007-06-14 | Sumitomo Chemical Company, Limited | ピリダジン化合物及びその用途 |
TWI372752B (en) | 2005-12-22 | 2012-09-21 | Nihon Nohyaku Co Ltd | Pyrazinecarboxamide derivatives and plant disease controlling agents containing the same |
JP2007217353A (ja) | 2006-02-17 | 2007-08-30 | Sankyo Agro Kk | 1,2,3,4−テトラヒドロキノリン化合物 |
TWI384949B (zh) * | 2006-12-01 | 2013-02-11 | 含有以喹啉化合物或其鹽為有效成分之土壤處理劑或種子處理劑、與使用彼等之植物病害之防治方法 | |
CN101311170B (zh) | 2007-05-25 | 2010-09-15 | 中国中化股份有限公司 | 取代嘧啶醚类化合物及其应用 |
UA99460C2 (ru) | 2007-06-01 | 2012-08-27 | Басф Се | Способ получения n-замещенных (3-дигалометил-1-метилпиразол-4-ил)карбоксамидов |
JP5631540B2 (ja) * | 2007-11-05 | 2014-11-26 | 石原産業株式会社 | 殺菌性組成物及び有害菌類の防除方法 |
PT2562162E (pt) | 2008-01-22 | 2015-10-21 | Dow Agrosciences Llc | Derivados de n-ciano-4-amino-5-fluoro-pirimidina como fungicidas |
JP5132446B2 (ja) | 2008-06-27 | 2013-01-30 | 三井化学アグロ株式会社 | 植物病害防除組成物及びそれを施用する植物病害の防除方法 |
EP2271219B1 (de) | 2008-10-15 | 2011-11-23 | Bayer CropScience AG | Verwendung von dithiin-tetracarboximiden zum bekämpfen phytopathogener pilze |
TW201031331A (en) | 2009-02-19 | 2010-09-01 | Bayer Cropscience Ag | Pesticide composition comprising a tetrazolyloxime derivative and a fungicide or an insecticide active substance |
AR076427A1 (es) | 2009-04-24 | 2011-06-08 | Basf Se | Compuestos de triazol que llevan un sustituyente de azufre ii |
AP2011006042A0 (en) | 2009-05-29 | 2011-12-31 | Syngenta Participations Ag | Substituted quinazolines as fungicides. |
KR20120046175A (ko) | 2009-06-18 | 2012-05-09 | 바스프 에스이 | 살진균 혼합물 |
JP5466893B2 (ja) | 2009-07-01 | 2014-04-09 | 三井化学アグロ株式会社 | キノリン系化合物を含有する植物病虫害防除剤および防除方法 |
US8507694B2 (en) | 2009-08-06 | 2013-08-13 | Syngenta Crop Protection Llc | Process for the preparation of pyrazole carboxylic acid amides |
TW201117722A (en) | 2009-11-04 | 2011-06-01 | Du Pont | Fungicidal mixtures |
UA108867C2 (uk) | 2009-12-08 | 2015-06-25 | Похідні азолу, спосіб їх одержання (варіанти), проміжні продукти, засіб для сільського господарства і садівництва | |
AU2009357098B2 (en) | 2009-12-22 | 2014-06-05 | Mitsui Chemicals Crop & Life Solutions, Inc. | Plant disease control composition and method for controlling plant disease by applying the same |
AU2011204323B2 (en) | 2010-01-07 | 2013-12-12 | E. I. Du Pont De Nemours And Company | Fungicidal heterocyclic compounds |
JP2011157294A (ja) * | 2010-01-29 | 2011-08-18 | Mitsui Chemicals Agro Inc | 有害生物防除組成物 |
TW201210488A (en) | 2010-08-09 | 2012-03-16 | Basf Se | Fungicidal mixtures |
TWI504350B (zh) | 2010-09-01 | 2015-10-21 | Du Pont | 殺真菌吡唑及其混合物 |
AR086961A1 (es) | 2011-06-17 | 2014-02-05 | Basf Se | Mezclas fungicidas sinergicas que comprenden 2,3,5,6-tetraciano-[1,4]ditiina |
US9090600B2 (en) | 2011-09-12 | 2015-07-28 | Bayer Intellectual Property Gmbh | Fungicidal 4-substituted-3-{phenyl[(heterocyclylmethoxy)imino]methyl}-1,2,4-oxadizol-5(4H)-one derivatives |
EP2735231A1 (en) | 2012-11-23 | 2014-05-28 | Bayer CropScience AG | Active compound combinations |
JP2014015470A (ja) * | 2013-09-03 | 2014-01-30 | Sumitomo Chemical Co Ltd | 有害生物防除組成物及びその用途 |
AR098031A1 (es) | 2013-10-16 | 2016-04-27 | Bayer Cropscience Ag | Combinaciones de compuestos activos que comprenden un derivado de (tio)carboxamida y un compuesto fungicida |
US20160330959A1 (en) * | 2014-02-19 | 2016-11-17 | Bayer Cropscience Aktiengesellschaft | Fungicidal compositions of pyrazolecarboxylic acid alkoxyamides |
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RU2016141053A3 (ja) | 2018-06-26 |
RU2016141053A (ru) | 2018-04-26 |
JP2017508765A (ja) | 2017-03-30 |
CN106132202B (zh) | 2021-12-31 |
WO2015141867A1 (en) | 2015-09-24 |
UA121030C2 (uk) | 2020-03-25 |
KR102324523B1 (ko) | 2021-11-09 |
PH12016501829B1 (en) | 2016-12-19 |
PH12016501829A1 (en) | 2016-12-19 |
TWI670010B (zh) | 2019-09-01 |
RU2673722C2 (ru) | 2018-11-29 |
US10201158B2 (en) | 2019-02-12 |
TW201600011A (zh) | 2016-01-01 |
CR20160478A (es) | 2017-01-02 |
KR20160134727A (ko) | 2016-11-23 |
MX2016012145A (es) | 2017-01-19 |
EP3119200A1 (en) | 2017-01-25 |
BR112016021563A2 (pt) | 2018-07-10 |
EP3119200A4 (en) | 2017-08-23 |
AR099795A1 (es) | 2016-08-17 |
CA2943184C (en) | 2023-04-04 |
BR112016021563B1 (pt) | 2021-12-21 |
AU2015232357A1 (en) | 2016-10-06 |
US20170094971A1 (en) | 2017-04-06 |
ECSP16082790A (es) | 2017-08-31 |
CA2943184A1 (en) | 2015-09-24 |
AU2015232357B2 (en) | 2018-06-14 |
AU2015232357C1 (en) | 2021-02-11 |
CA3187573A1 (en) | 2015-09-24 |
CL2016002254A1 (es) | 2017-06-23 |
MY189356A (en) | 2022-02-07 |
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