JP2013509379A - 除草剤テトラヒドロフタルイミド - Google Patents
除草剤テトラヒドロフタルイミド Download PDFInfo
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- JP2013509379A JP2013509379A JP2012535828A JP2012535828A JP2013509379A JP 2013509379 A JP2013509379 A JP 2013509379A JP 2012535828 A JP2012535828 A JP 2012535828A JP 2012535828 A JP2012535828 A JP 2012535828A JP 2013509379 A JP2013509379 A JP 2013509379A
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- formula
- methyl
- tetrahydrophthalimide
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- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- AZHZOGYUMMIAOF-UHFFFAOYSA-N trifludimoxazin Chemical compound O=C1N(C)C(=S)N(C)C(=O)N1C(C(=C1)F)=CC2=C1OC(F)(F)C(=O)N2CC#C AZHZOGYUMMIAOF-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 239000002753 trypsin inhibitor Substances 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000009105 vegetative growth Effects 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Abstract
Description
R1は、水素又はハロゲンであり;
R2は、水素、C1〜C6−アルキル、C1〜C6−ハロアルキル、C3〜C6−シクロアルキル、C3〜C6−アルケニル、C3〜C6−ハロアルケニル、C3〜C6−アルキニル、C3〜C6−ハロアルキニル、C1〜C6−アルコキシ又はC3〜C6−シクロアルキル−C1〜C6−アルキルであり;
R3は、ハロゲンであり;
R4は、ハロゲン(好ましくはフッ素)であり;
Wは、O又はSである]
で表されるテトラヒドロフタルイミドを提供するものである。
・ C1〜C4−アルキル並びにC3〜C6−シクロアルキル−C1〜C4−アルキルのC1〜C4−アルキル部分:例えばCH3、C2H5、n−プロピル、並びにCH(CH3)2、n−ブチル、CH(CH3)−C2H5、CH2−CH(CH3)2及びC(CH3)3;
である。
R1は水素であり、
また好ましくはハロゲン、特に好ましくはF又はClであり(非常に好ましいのはF);
R2はC3〜C6−アルキニル又はC3〜C6−ハロアルキニル、好ましくはC3−アルキニル又はC3−ハロアルキニル、特に好ましくはCH2C≡CH、CH2C≡CCl又はCH2C≡CBrであり、
また好ましくはC3〜C6−アルキニル又はC3〜C6−シクロアルキル−C1〜C6−アルキル、特に好ましくはプロパルギル又はシクロプロピルメチルであり、
また好ましくはC3〜C6−アルキニル、好ましくはC3−アルキニルであり、特に好ましくはCH2C≡CHであり、
また好ましくはC3〜C6−ハロアルキニル、好ましくはC3−ハロアルキニル、特に好ましくはCH2C≡CCl又はCH2C≡CBrであり;
R3はFであり;
R4はFであり;
WはOであり、
また好ましくはSである;
で表されるテトラヒドロフタルイミドとも呼ばれる。
アリウム・セパ[Allium cepa;タマネギ]、アナナス・コモスス[Ananas comosus;パイナップル]、アラキス・ヒポゲア[Arachis hypogaea;ラッカセイ]、アスパラガス・オフィチナリス[Asparagus officinalis;アスパラガス]、アベナ・サチバ[Avena sativa;エンバク]、ベータ・ブルガリス品種アルチシマ[Beta vulgaris spec. altissima;テンサイ]、ベータ・ブルガリス品種ラパ[Beta vulgaris spec. rapa;サトウダイコン]、ブラッシカ・ナプス変種ナプス[Brassica napus var. napus;セイヨウアブラナ]、ブラッシカ・ナプス変種ナポブラッシカ[Brassica napus var. napobrassica;セイヨウキャベツ]、ブラッシカ・ラパ変種シルベストリス[Brassica rapa var. silvestris;インドアブラナ]、ブラッシカ・オレラセア[Brassica oleracea;セイヨウキャベツ]、ブラッシカ・ニグラ[Brassica nigra;クロガラシ]、カメリア・シネンシス[Camellia sinensis;チャ]、カルタムス・チンクトリウス[Carthamus tinctorius;ベニバナ]、カルヤ・イリノイネンシス[Carya illinoinensis;ペカン]、シトルス・リモン[Citrus limon;レモン]、シトルス・シネンシス[Citrus sinensis;オレンジスウィート]、コフェア・アラビカ[Coffea arabica;アラビアコーヒーノキ)(コフェア・カネフォラ[Coffea canephora;ロブスタコーヒーノキ]、コフェア・リベリカ[Coffea liberica;リベリアコーヒーノキ])、ククミス・サチバス[Cucumis sativus;キュウリ]、シノドン・デクチドン[Cynodon dactylon;ギョウギシバ]、ダウカス・カロタ[Daucus carota;ニンジン]、エラエイス・ギネエンシス[Elaeis guineensis;アブラヤシ]、フラガリア・ベスカ[Fragaria vesca;イチゴ]、グリシン・マクス[Glycine max;ダイズ]、ゴシッピウム・ヒルスツム[Gossypium hirsutum;リクチワタ](ゴシピウム・アルボレウム[Gossypium arboreum;キダチワタ]、ゴシピウム・ヘルバケウム[Gossypium herbaceum;アジアワタ]、ゴシピウム・ビチフォリウム[Gossypium vitifolium;ウミシマワタ])、ヘリアンタス・アヌウス[Helianthus annuus;ヒマワリ]、ヘベア・ブラシリエンシス[Hevea brasiliensis;パラゴムノキ]、ホルデウム・ブルガレ[Hordeum vulgare;オオムギ]、フムラス・ルプルス[Humulus lupulus;ホップ]、イポモエア・バタタス[Ipomoea batatas;サツマイモ]、ジュグランス・レギア[Juglans regia;シナノグルミ]、レンス・クリナリス[Lens culinaris;ヒラマメ]、リヌム・ウシタチシマム[Linum usitatissimum;アマ]、リコペルシコン・リコペルシカム[Lycopersicon lycopersicum;トマト]、マルス・品種[Malus spec.;リンゴ属品種]、マニホット・エスクレンタ[Manihot esculenta;キャッサバ]、メジカゴ・サチバ[Medicago sativa;アルファルファ]、ムサ・品種[Musa spec.;バナナ属品種]、ニコチアナ・タバクム[Nicotiana tabacum;タバコ](ニコチアナ・ルスチカ[Nicotiana rustica;マルバタバコ])、オレア・エウロペア[Olea europaea;オリーブ]、オリザ・サチバ[Oryza sativa;イネ]、ファセオラス・ルナタス[Phaseolus lunatus;ライマメ]、ファセオラス・ブルガリス[Phaseolus vulgaris;インゲンマメ]、ピセア・アビエス[Picea abies;ドイツトウヒ]、ピナス・品種[Pinus spec.;マツ属品種]、ピスタシア・ベラ[Pistacia vera;ピスタシオノキ]、ピスム・サチバム[Pisum sativum;エンドウ]、プルナス・アビウム[Prunus avium;セイヨウウミザクラ]、プルナス・ペルシカ[Prunus persica;モモ]、ピルス・コムニス[Pyrus communis;セイヨウナシ]、プルヌス・アルメニアカ[Prunus armeniaca;アンズ]、プルヌス・サラスス[Prunus cerasus;サクラ]、プルヌス・デュルシス[Prunus dulcis;アーモンド]、プルヌス・ドメスチカ[Prunus domestica;プルーン]、リベス・シルベストレ[Ribes sylvestre;フサスグリ]、リシナス・コムニス[Ricinus communis;ヒマ]、サッカラム・オフィシナルム[Saccharum officinarum;サトウキビ]、セカレ・セレアレ[Secale cereale;ライムギ]、シナピス・アルバ[Sinapis alba;シロガラシ]、ソラナム・ツベロサム[Solanum tuberosum;ジャガイモ]、ソルガム・ビコロル[Sorghum bicolor;モロコシ](ソルガム・ブルガレ[Sorghum vulgare;ホウキモロコシ])、テオブロマ・カカオ[Theobroma cacao;カカオ]、トリフォリウム・プラテンセ[Trifolium pratense;アカツメクサ]、トリチクム・アエスチバム[Triticum aestivum;コムギ]、トリチカレ[Triticale;ライコムギ]、トリチクム・デュラム[Triticum durum;マカロニコムギ]、ビシア・ファバ[Vicia faba;ソラマメ]、ビティス・ビニフェラ[Vitis vinifera;ブドウ]、及びゼア・マイス[Zea mays;トウモロコシ]。
A 液剤(Water-soluble concentrates)
10重量部の活性化合物を90重量部の水又は水可溶溶媒に溶解させる。別法として、湿潤剤又は他の補佐剤を加える。活性化合物は水で希釈すると同時に溶解する。これにより活性化合物含有量が10重量%の製剤が得られる。
20重量部の活性化合物を10重量部の分散剤(例えばポリビニルピロリドン)を加えてある70重量部のシクロヘキサノンに溶解させる。水で希釈すると同時にディスパージョンが得られる。活性化合物含有量は20重量%である。
15重量部の活性化合物をドデシルベンゼンスルホン酸カルシウムとヒマシ油エトキシラートを加えてある(各場合5重量部)75重量部の有機溶媒(例えばアルキル芳香族)に溶解させる。水で希釈するとエマルションが得られる。この製剤は15重量%の活性化合物含有量を有している。
25重量部の活性化合物をドデシルベンゼンスルホン酸カルシウムとヒマシ油エトキシラートを加えてある(各場合5重量部)35重量部の有機溶媒(例えばアルキル芳香族)に溶解させる。この混合物を乳化装置(例えばUltraturrax)を用いて30重量部の水に導入して均質なエマルションにする。水で希釈するとエマルションが得られる。この製剤は25重量%の活性化合物含有量を有している。
撹拌下にあるボールミル中で、20重量部の活性化合物を10重量部の分散剤+湿潤剤及び70重量部の水又は有機溶媒を加えて粉砕して微細活性化合物懸濁液を得る。水で希釈すると活性化合物の安定懸濁液が得られる。製剤中の活性化合物含有量は20重量%である。
専用の装置(例えば押出機、噴霧塔、流動床)を用いて50重量部の活性化合物を50重量部の分散剤+湿潤剤を加えて細かく粉砕して顆粒水和剤又は顆粒水溶剤にする。水で希釈すると活性化合物の安定なディスパージョン又は溶液が得られる。この製剤は50重量%の活性化合物含有量を有している。
75重量部の活性化合物をローター・ステーター・ミル中で25重量部の分散剤+湿潤剤+シリカゲルを加えて粉砕する。水で希釈すると活性化合物の安定なディスパージョン又は溶液が得られる。この製剤の活性化合物含有量は75重量%である。
ボールミル中で、20重量部の活性化合物、10重量部の分散剤、1重量部のゲル化剤及び70重量部の水又は有機溶媒を混合して微細懸濁液を得る。水で希釈すると活性化合物含有量が20重量%の安定な懸濁液が得られる。
I 粉末剤(Dusts)
5重量部の活性化合物を細かく粉砕して95重量部の微粉砕カオリンと緊密に混合する。これにより活性化合物含有量が5重量%の散粉用粉粒が得られる。
0.5重量部の活性化合物を細かく粉砕して99.5重量部の担体と組み合わせる。この場合の現代流方法は、押出、噴霧乾燥又は流動床である。これにより活性化合物含有量が0.5重量%の希釈せずに適用される顆粒剤が得られる。
10重量部の活性化合物を90重量部の有機溶媒(例えばキシレン)に溶解させる。これにより活性化合物含有量が10重量%の希釈せずに適用される調製品が得られる。
b1) 脂質生合成阻害剤;
b2) アセトラクタートシンターゼ阻害剤(ALS阻害剤);
b3) 光合成阻害剤;
b4) プロトポルフィリノゲン−IXオキシダーゼ阻害剤;
b5) 白化除草剤;
b6) エノルピルビルシキマート3−ホスファートシンターゼ阻害剤(EPSP阻害剤);
b7) グルタミンシンテターゼ阻害剤;
b8) 7,8−ジヒドロプテロアートシンターゼ阻害剤(DHP阻害剤);
b9) 有糸***阻害剤;
b10) 極長鎖脂肪酸合成阻害剤(VLCFA阻害剤);
b11) セルロース生合成阻害剤;
b12) デカップラー型除草剤;
b13) オーキシン型除草剤;
b14) オーキシン輸送阻害剤;及び
b15) ブロモブチド、クロルフルレノール、クロルフルレノール−メチル、シンメチリン、クミルウロン、ダラポン、ダゾメト、ジフェンゾコート、ジフェンゾコート−メチルスルファート、ジメチピン、DSMA、ジムロン、エンドタール及びその塩、エトベンザニド、フランプロプ、フランプロプ−イソプロピル、フランプロプ−メチル、フランプロプ−M−イソプロピル、フランプロプ−M−メチル、フルレノール、フルレノール−ブチル、フルルプルイミドール、ホサミン、ホサミン−アンモニウム、インダノファン、インダジフラム、マレイン酸ヒドラジド、メフルイジド、メタム、メチルアジド、メチルブロミド、メチル−ジムロン、ヨウ化メチル、MSMA、オレイン酸、オキサジクロメホン、ペラルゴン酸、ピリブチカルブ、キノクラミン、トリ−アジフラム、トリジファン及び6−クロロ−3−(2−シクロプロピル−6−メチルフェノキシ)−4−ピリダジノール(CAS499223−49−3)及びその塩並びにエステルからなる群から選択される他の除草剤。
b1)以下の脂質生合成阻害剤の群から選択されるもの:
ACC系除草剤、例えばアロキシジム、アロキシジム−ナトリウム、ブトロキシジム、クレトジム、クロジナホプ、クロジナホプ−プロパルギル、シクロキシジム、シハロホプ、シハロホプ−ブチル、ジクロホプ、ジクロホプ−メチル、フェノキサプロプ、フェノキサプロプ−エチル、フェノキサプロプ−P、フェノキサプロプ−P−エチル、フルアジホプ、フルアジホプ−ブチル、フルアジホプ−P、フルアジホプ−P−ブチル、ハロキシホプ、ハロキシホプ−メチル、ハロキシホプ−P、ハロキシホプ−P−メチル、メタミホプ、ピノキサデン、プロホキシジム、プロパキザホプ、キザロホプ、キザロホプ−エチル、キザロホプ−テフリル、キザロホプ−P、キザロホプ−P−エチル、キザロホプ−P−テフリル、セトキシジム、テプラロキシジム及びトラルコキシジム、さらには非ACC系除草剤、例えばベンフレサート、ブチラート、シクロアート、ダラポン、ジメピペラート、EPTC、エスプロカルブ、エトフメサート、フルプロパナート、モリナート、オルベンカルブ、ペブラート、プロスルホカルブ、TCA、チオベンカルブ、チオカルバジル、トリアラート及びベルノラート;
スルホニル尿素系、例えばアミドスルフロン、アジムスルフロン、ベンスルフロン、ベンスルフロン−メチル、クロリムロン、クロリムロン−エチル、クロルスルフロン、シノスルフロン、シクロスルファムロン、エタメトスルフロン、エタメトスルフロン−メチル、エトキシスルフロン、フラザスルフロン、フルセトスルフロン、フルピルスルフロン、フルピルスルフロン−メチル−ナトリウム、ホラムスルフロン、ハロスルフロン、ハロスルフロン−メチル、イマゾスルフロン、ヨードスルフロン、ヨードスルフロン−メチル−ナトリウム、メソスルフロン、メタゾスルフロン、メトスルフロン、メトスルフロン−メチル、ンイコスルフロン、オルトスルファムロン、オキサスルフロン、プリミスルフロン、プリミスルフロン−メチル、プロピリスルフロン、プロスルフロン、ピラゾスルフロン、ピラゾスルフロン−エチル、リムスルフロン、スルホメツロン、スルホメツロン−メチル、スルホスルフロン、チフェンスルフロン、チフェンスルフロン−メチル、トリアスルフロン、トリベヌロン、トリベヌロン−メチル、トリフロキシスルフロン、トリフルスルフロン、トリフルスルフロン−メチル及びトリトスルフロン、イミダゾリノン系、例えばイマザメタベンゾ、イマザメタベンゾ−メチル、イマザモックス、イマザピック、イマザピル、イマザキン及びイマゼタピル、トリアゾロピリミジン系除草剤並びにスルホンアニリド系、例えばクロランスラム、クロランスラム−メチル、ジクロスラム、フルメツラム、フロラスラム、メトスラム、ペノキッスラム、ピリミスルファン及びピロキッスラム、ピリミジニルベンゾアート系例えばビスピリバク、ビスピリバク−ナトリウム、ピリベンゾオキシム、ピリフタリド、ピリミノバク、ピリミノバク−メチル、ピリチオバク、ピリチオバク−ナトリウム、4−[[[2−[(4,6−ジメトキシ−2−ピリミジニル)オキシ]フェニル]メチル]アミノ]−安息香酸−1−メチルエチルエステル(CAS420138−41−6)、4−[[[2−[(4,6−ジメトキシ−2−ピリミジニル)オキシ]フェニル]メチル]アミノ]−安息香酸プロピルエステル(CAS420138−40−5)、N−(4−ブロモフェニル)−2−[(4,6−ジメトキシ−2−ピリミジニル)オキシ]ベンゼンメタンアミン(CAS420138−01−8)並びにスルホニルアミノカルボニル−トリアゾリノン系除草剤、例えばフルカルバゾン、フルカルバゾン−ナトリウム、プロポキシカルバゾン、プロポキシカルバゾン−ナトリウム、チエンカルバゾン及びチエンカルバゾン−メチル(これらの中でも、本発明の好ましい実施形態は、少なくとも1種のイミダゾリノン系除草剤を含んでいる組成物に関係する);
アミカルバゾン、光化学系IIの阻害剤、例えばトリアジン系除草剤(クロロトリアジン、トリアジノン系、トリアジンジオン系、メチルチオトリアジン系及びピリダジノン系の除草剤を含めて)例えばアメトリン、アトラジン、クロリダゾン、シアナジン、デスメトリン、ジメタメトリン、ヘキサジノン、ムトリブジン、プロメトン、プロメトリン、プロパジン、シマジン、シメトリン、テルブメトン、テルブチルアジン、テルブトリン及びトリエタジン、アリール尿素系クロロブロムロン、クロロトルロン、クロロキスロン、ジメフロン、ジウロン、フルオメツロン、イソプロツロン、イソウロン、リヌロン、メタミトロン、メタベンズチアズロン、メトベンズロン、メトキスロン、モノリヌロン、ネブロン、シズロン、トブチウロン及びチアジアズロン、フェニルカルバマート系、例えばデスムジファム、カルブチラト、フェンムジファム、フェンムジファム−エチル、ニトリル系除草剤、例えばブロモフェノキシム、ブロモキシニル及びその塩並びにエステル、イオキシニル及びその塩並びにエステル、ウラシル系、例えばブロマシル、レナシル及びテルバシル、さらにはベンタゾン並びにベンタゾン−ナトリウム、ピリダート、ピリダホール、ペンタノクロル及びプロプアニル、及び、光化学系Iの阻害剤、例えばジコート、ジコート−ジブロミド、パラコート、パラコート−ジクロリド及びパラコート−ジメチルスルファート(これらの中でも、本発明の好ましい実施形態は、少なくとも1種のアリール尿素系除草剤を含んでいる組成物に関し;これらの中でも、同様に、本発明の好ましい実施形態は、少なくとも1種のトリアジン系除草剤を含んでいる組成物に関し;これらの中でも、同様に、本発明の好ましい実施形態は、少なくとも1種のニトリル系除草剤を含んでいる組成物に関係する);
アシフルオルフェン、アシフルオルフェン−ナトリウム、アザフェニジン、ベンカルバゾン、ベンズフェンジゾン、ビフェノキス、ブタフェナシル、カルフェントラゾン、カルフェントラゾン−エチル、クロメトキシフェン、シニドン−エチル、フルアゾラート、フルフェンピル、フルフェンピル−エチル、フルミクロラク、フルミクロラク−ペンチル、フルミオキサジン、フルオログリコフェン、フルオログリコフェン−エチル、フルチアセト、フルチアセト−メチル、ホメサフェン、ハロサフェン、ラクトフェン、オキサジアルギル、オキサジアゾン、オキシフルオルフェン、ペントキサゾン、プロフルアゾール、ピラクロニル、ピラフルフェン、ピラフルフェン−エチル、サフルフェナシル、スルフェントラゾン、チジアジミン、エチル[3−[2−クロロ−4−フルオロ−5−(1−メチル−6−トリフルオロメチル−2,4−ジオキソ−1,2,3,4−テトラヒドロピリミジン−3−イル)フェノキシ]−2−ピリジルオキシ]アセタート(CAS353292−31−6;S−3100)、N−エチル−3−(2,6−ジクロロ−4−トリフルオロメチルフェノキシ)−5−メチル−1H−ピラゾール−1−カルボキサミド(CAS452098−92−9)、N−テトラヒドロフルフリル−3−(2,6−ジクロロ−4−トリフルオロメチルフェノキシ)−5−メチル−1H−ピラゾール−1−カルボキサミド(CAS915396−43−9)、N−エチル−3−(2−クロロ−6−フルオロ−4−トリフルオロメチルフェノキシ)−5−メチル−1H−ピラゾール−1−カルボキサミド(CAS452099−05−7)、N−テトラヒドロフルフリル−3−(2−クロロ−6−フルオロ−4−トリフルオロメチルフェノキシ)−5−メチル−1H−ピラゾール−1−カルボキサミド(CAS45100−03−7)、3−[7−フルオロ−3−オキソ−4−(プロプ−2−イニル)−3,4−ジヒドロ−2H−ベンゾ[1,4]オキサジン−6−イル]−1,5−ジメチル−6−チオキソ−[1,3,5]トリアジナン−2,4−ジオン、さらには1,5−ジメチル−6−チオキソ−3−(2,2,7−トリフルオロ−3−オキソ−4−(プロプ−2−イニル)−3,4−ジヒドロ−2H−ベンゾ[b][1,4]オキサジン−6−イル)−1,3,5−トリアジナン−2,4−ジオン;
PDS阻害剤:ベフルブトアミド、ジフルフェニカン、フルリドン、フルロクロリドン、フルルタモン、ノルフルラゾン、ピコリナフェン、さらには4−(3−トリフルオロメチルフェノキシ)−2−(4−トリフルオロメチルフェニル)ピリミジン(CAS180608−33−7)、HPPD阻害剤:ベンゾビシクロン、ベンゾフェナプ、イソキサフルトール、メソトリオン、ピラスルホトール、ピラゾリナート、ピラゾキシフェン、スルコトリオン、テフリルトリオン、テンボトリオン、トプラメゾン及びビシクロピロン、白化剤(標的不明):アクロニフェン、アミトロール、クロマゾン及びフルメツロン;
グリホサート、グリホサート−イソプロピルアンモニウム及びグリホサート−トリメシウム(スルホサート);
ビラナホス(ビアラホス)、ビラナホス−ナトリウム、グルホシナート、グルホシナート−P及びグルホシナート−アンモニウム;
アスラム;
群K1の化合物:ジニトロアニリン系、例えばベンフルラリン、ブトラリン、ジニトロアミン、エタルフルラリン、フルクロラリン、オリザリン、ペンジメタリン、プロジアミン及びトリフルラリン、ホスホルアミダート系、例えばアミプロホス、アミプロホス−メチル、さらにはブタミホス、安息香酸系除草剤、例えばクロルタール、クロルタール−ジメチル、ピリジン系、例えばジチオピル及びチアゾピル、ベンズアミド系、例えばプロピズアミド及びトブタム;群K2の化合物:クロルプロファム、プロファム及びカルベトアミド(これらの中でも、群K1の化合物、特にはジニトロアニリン系が好ましい);
クロロアセトアミド系、例えばアセトクロル、アラクロル、ブタクロル、ジメタクロル、ジメテンアミド、ジメテンアミド−P、メタザクロル、メトラクロル、メトラクロル−S、ペトキサミド、プレチラクロル、プロパクロル、プロピソクロル及びテニルクロル、オキシアセトアニリド系、例えばフルフェンアセト及びメフェンアセト、アセトアニリド系、例えばジフェンアミド、ナプロアニリド及びナプロプアミド、テトラゾリノン系、例えばフェントラズアミド、さらには他の除草剤系、例えばアニロホス、カフェンストロール、フェノキサスルホン、イペンカルバゾン、ピペロホス、ピロキサスルホン並びに式II
R21、R22、R23、R24 互いに独立して水素、ハロゲン又はC1〜C4−アルキル;
W 環員として酸素、窒素及びイオウから選択される1、2又は3個の同じ又は異なるヘテロ原子を、炭素環員に加えて含有しているフェニル又は単環式5、6、7、8、9もしくは10員へテロシクリル(このフェニル及びヘテロシクリルは不置換であるか又はハロゲン、C1〜C4−アルキル、C1〜C4−アルコキシ、C1〜C4−ハロアルキル及びC1〜C4−ハロアルコキシから選択される1、2又は3個の置換基Ryyを有している)、好ましくは環員として1、2又は3個の窒素原子を、炭素環員に加えて含有しているフェニル又は5もしくは6員芳香族へテロシクリル(ヘタリール)(このフェニル及びヘタリールは不置換であるか又は1、2又は3個の置換基Ryyを有している);
Z 酸素又はNH;
n 0又は1]
で表されるイソオキサゾリン化合物;
R21、R22、R23、R24は互いに独立してH、F、Cl又はメチルである;
Zは酸素である;
nは0又は1である;
Wはフェニル、ピラゾリル又は1,2,3−トリアゾリルである(この最後に言及した3基は不置換であるか又は1、2又は3個の置換基Ryy、特には以下の各基
R22は、ハロゲン、C1〜C4−アルキル又はC1〜C4−ハロアルキルであり;
R26は、C1〜C4−アルキルであり;
R27は、ハロゲン、C1〜C4−アルコキシ又はC1〜C4−ハロアルコキシであり;
R28は、ハロゲン、C1〜C4−アルキル、C1〜C4−ハロアルキル又はC1〜C4−ハロアルコキシであり;
mは、0、1、2又は3であり;
#は、基CR23R24への結合点を表している]
のうちの1つを有している);
式IIで表されるイソオキサゾリン化合物であり、
R21は水素である;
R22はフッ素である;
R23は水素又はフッ素である;
R24は水素又はフッ素である;
Wは、式W1、W2、W3又はW4
で表される各基のうちの1つである;
Zは酸素である;
nは0又は1(特には1)である;
式IIで表されるイソオキサゾリン化合物であり、
クロルチアミド、ジクロベニル、フルポキサム、イソキサベン、1−シクロへキシル−5−ペンタフルオルフェニルオキシ−14−[1,2,4,6]チアトリアジン−3−イルアミン並びに式III
Aは、フェニル又はピリジル(ここで、Raは、Aの炭素原子への結合点に対してオルト位に結合されている)であり;
Raは、CN、NO2、C1〜C4−アルキル、D−C3〜C6−シクロアルキル、C1〜C4−ハロアルキル、C1〜C4−アルコキシ、C1〜C4−ハロアルコキシ、O−D−C3〜C6−シクロアルキル、S(O)qRy、C2〜C6−アルケニル、D−C3〜C6−シクロアルケニル、C3〜C6−アルケニルオキシ、C2〜C6−アルキニル、C3〜C6−アルキニルオキシ、NRARB、トリ−C1〜C4−アルキルシリル、D−C(=O)−Ra1、D−P(=O)(Ra1)2、フェニル、ナフチルであり、
O、N及びSからなる群から選択される1、2、3又は4個のへテロ原子を含有していて、基Raa及び/又はRa1、並びに、Raが炭素原子に結合されている場合は、さらにはハロゲンによって部分的又は完全に置換されていてよい、炭素又は窒素を介して結合されている3〜7員単環式又は9もしくは10員二環式飽和、不飽和もしくは芳香族へテロ環であり、
Ryは、C1〜C6−アルキル、C3〜C4−アルケニル、C3〜C4−アルキニル、NRARB又はC1〜C4−ハロアルキルであり、qは0、1又は2であり、
RA、RBは、互いに独立して、水素、C1〜C6−アルキル、C3〜C6−アルケニル及びC3〜C6−アルキニルであり;それらが結合されている窒素原子と一緒になって、RA、RBは、O、N及びSからなる群から選択される1、2又は3個のへテロ原子を、炭素原子に加えて含有していてよい5もしくは6員飽和、部分又は完全不飽和環を形成していてもよく、この環は1〜3個の基Raaで置換されていてよく、
Dは、共有結合、C1〜C4−アルキレン、C2〜C6−アルケニル又はC2〜C6−アルキニルであり、
Ra1は、水素、OH、C1〜C8−アルキル、C1〜C4−ハロアルキル、C3〜C6−シクロアルキル、C2〜C8−アルケニル、C5〜C6−シクロアルケニル、C2〜C8−アルキニル、C1〜C6−アルコキシ、C1〜C4−ハロアルコキシ、C3〜C8−アルケニルオキシ、C3〜C8−アルキニルオキシ、NRARB、C1〜C6−アルコキシアミノ、C1〜C6−アルキルスルホニルアミノ、C1〜C6−アルキルアミノスルホニルアミノ、[ジ−(C1〜C6)アルキルアミノ]スルホニルアミノ、C3〜C6−アルケニルアミノ、C3〜C6−アルキニルアミノ、N−(C2〜C6−アルケニル)−N−(C1〜C6−アルキル)アミノ、N−(C2〜C6−アルキニル)−N−(C1〜C6−アルキル)アミノ、N−(C1〜C6−アルコキシ)−N−(C1〜C6−アルキル)アミノ、N−(C2〜C6−アルケニル)−N−(C1〜C6−アルコキシ)アミノ、N−(C2〜C6−アルキニル)−N−(C1〜C6−アルコキシ)−アミノ、C1〜C6−アルキルスルホニル、トリ−C1〜C4−アルキルシリル、フェニル、フェノキシ、フェニルアミノ、又は
O、N及びSからなる群から選択される1、2、3又は4個のへテロ原子を含有している5もしくは6員単環式又は9もしくは10員二環式へテロ環(ここで、この環式基は、不置換であるか又は1、2、3又は4個の基Raaで置換されている)であり、
Raaは、ハロゲン、OH、CN、NO2、C1〜C4−アルキル、C1〜C4−ハロアルキル、C1〜C4−アルコキシ、C1〜C4−ハロアルコキシ、S(O)qRy、D−C(=O)−Ra1及びトリ−C1〜C4−アルキルシリルであり;
Rbは、互いに独立して、水素、CN、NO2、ハロゲン、C1〜C4−アルキル、C1〜C4−ハロアルキル、C2〜C4−アルケニル、C3〜C6−アルキニル、C1〜C4−アルコキシ、C1〜C4−ハロアルコキシ、ベンジル又はS(O)qRyであり、
Rbは、隣接環原子に結合されている基Ra又はRbと一緒になって、O、N及びSからなる群から選択される1、2又は3個のへテロ原子を、炭素原子に加えて含有していてよい5もしくは6員飽和又は部分もしくは完全不飽和環を形成していてもよく(この環はRaaによって部分的又は完全に置換されていてよい);
pは、0、1、2又は3であり;
R30は、水素、OH、CN、C1〜C12−アルキル、C3〜C12−アルケニル、C3〜C12−アルキニル、C1〜C4−アルコキシ、C3〜C6−シクロアルキル、C5〜C6−シクロアルケニル、NRARB、S(O)nRy、S(O)nNRARB、C(=O)R40、CONRARB、フェニル、又は
O、N及びSからなる群から選択される1、2、3又は4個のへテロ原子を含有している5もしくは6員単環式又は9もしくは10員二環式芳香族へテロ環(ここで、この環式基はD1を介して結合されていて、不置換であるか又は1、2、3又は4個の基Raa、並びに以下の部分又は完全Raa−置換基:C1〜C4−アルキル、C3〜C4−アルケニル及びC3〜C4−アルキニルで置換されている)であり、
R40は、水素、C1〜C4−アルキル、C1〜C4−ハロアルキル、C1〜C4−アルコキシ又はC1〜C4−ハロアルコキシであり、
D1は、カルボニル又は基Dであり、
ここで、基R30、Ra並びにそれらの従属置換基においては、その炭素鎖及び/又は環式基は、1、2、3又は4個の置換基Raa及び/又はRa1を有していてよく;
R31は、C1〜C4−アルキル、C3〜C4−アルケニル又はC3〜C4−アルキニルであり;
R32は、OH、NH2、C1〜C4−アルキル、C3〜C6−シクロアルキル、C3〜C6−アルケニル、C3〜C6−アルキニル、C1〜C4−ヒドロキシアルキル、C1〜C4−シアノアルキル、C1〜C4−ハロアルキル、C1〜C4−アルコキシ−C1〜C4−アルキル又はC(=O)R40であり;
R33は、水素、ハロゲン、C1〜C4−アルキル又はC1〜C4−ハロアルキルであり、又はR33及びR34は一緒になって共有結合であり;
R34、R35、R36、R37は、互いに独立して、水素、ハロゲン、OH、CN、NO2、C1〜C4−アルキル、C1〜C4−ハロアルキル、C2〜C6−アルケニル、C2〜C6−アルキニル、C1〜C4−アルコキシ、C1〜C4−ハロアルコキシ、C3〜C6−シクロアルキル、C3〜C6−シクロアルケニル及びC3〜C6−シクロアルキニルであり;
R38、R39は、互いに独立して、水素、ハロゲン、OH、ハロアルキル、NRARB、NRAC(O)R41、CN、NO2、C1〜C4−アルキル、C1〜C4−ハロアルキル、C2〜C4−アルケニル、C3〜C6−アルキニル、C1〜C4−アルコキシ、C1〜C4−ハロアルコキシ、O−C(O)R41、フェノキシ又はベンジルオキシであり(ここで、基R38及びR39においては、その炭素鎖及び/又は環式基は1、2、3又は4個の置換基Raaを有していてよい);
R41は、C1〜C4−アルキル又はNRARBである]
で表されるピペラジン化合物;
Aはフェニル又はピリジル(ここで、Raは、Aの炭素原子への結合点に対してオルト位に結合されている)である;
RaはCN、NO2、C1〜C4−アルキル、C1〜C4−ハロアルキル、C1〜C4−アルコキシ、C1〜C4−ハロアルコキシ又はD−C(=O)−Ra1であり、
RyはC1〜C6−アルキル、C3〜C4−アルケニル、C3〜C4−アルキニル、NRARB又はC1〜C4−ハロアルキルであり、qは0、1又は2であり、
RA、RBは、互いに独立して、水素、C1〜C6−アルキル、C3〜C6−アルケニル及びC3〜C6−アルキニルであり;それらが結合されている窒素原子と一緒になって、RA、RBは、O、N及びSからなる群から選択される1、2又は3個のへテロ原子を、炭素原子に加えて含有していてよい5もしくは6員飽和、部分又は完全不飽和環を形成していてもよく(この環は1〜3個の基Raaで置換されていてよい)、
Dは共有結合又はC1〜C4−アルキレンであり、
Ra1は水素、OH、C1〜C8−アルキル、C1〜C4−ハロアルキル、C3〜C6−シクロアルキルであり、
Raaはハロゲン、OH、CN、NO2、C1〜C4−アルキル、C1〜C4−ハロアルキル、C1〜C4−アルコキシ、C1〜C4−ハロアルコキシ、S(O)qRy、D−C(=O)−Ra1及びトリ−C1〜C4−アルキルシリルである;
Rbは、互いに独立して、CN、NO2、ハロゲン、C1〜C4−アルキル、C1〜C4−ハロアルキル、C2〜C4−アルケニル、C3〜C6−アルキニル、C1〜C4−アルコキシ、C1〜C4−ハロアルコキシ、ベンジル又はS(O)qRyであり、
Rbは、隣接環原子に結合されている基Ra又はRbと一緒になって、O、N及びSからなる群から選択される1、2又は3個のへテロ原子を、炭素原子に加えて含有していてよい5もしくは6員飽和又は部分もしくは完全不飽和環を形成していてもよい(この環はRaaによって部分的又は完全に置換されていてよい);
pは0又は1である;
R30は水素、C1〜C12−アルキル、C3〜C12−アルケニル、C3〜C12−アルキニル、C1〜C4−アルコキシ又はC(=O)R40であり、
R40は水素、C1〜C4−アルキル、C1〜C4−ハロアルキル、C1〜C4−アルコキシ又はC1〜C4−ハロアルコキシであり、
ここで、基R30、Ra並びにそれらの従属置換基においてはその炭素鎖及び/又は環式基は1、2、3又は4個の置換基Raa及び/又はRa1を有していてよい;
R31はC1〜C4−アルキルである;
R32はOH、NH2、C1〜C4−アルキル、C3〜C6−シクロアルキル、C1〜C4−ハロアルキル又はC(=O)R25である;
R33は水素であるか、又はR33とR34は一緒になって共有結合である;
R34、R35、R36、R37は互いに独立して水素である;
R38、R39は互いに独立して水素、ハロゲン又はOHである;
式IIIで表されるピペラジン化合物である;
ジノセブ、ジノテルブ及びDNOC並びにその塩;
2,4−D及びその塩並びにエステル、2,4−DB及びその塩並びにエステル、アミノピラリド及びその塩例えばアミノピラリド−トリス(2−ヒドロキシプロピル)アンモニウム及びその塩、ベナゾリン、ベナゾリン−エチル、クロランベン及びその塩並びにエステル、クロムプロプ、クロピラリド及びその塩並びにエステル、ジカンバ及びその塩並びにエステル、ジクロルプロプ及びその塩並びにエステル、ジ−クロルプロプ−P及びその塩並びにエステル、フルロキシピル、フルロキシピル−ブトメチル、フルロキシピル−メプチル、MCPA及びその塩並びにエステル、MCPA−チオエチル、MCPB及びその塩並びにエステル、メコプロプ及びその塩並びにエステル、メコプロプ−P及びその塩並びにエステル、ピクロラム及びその塩並びにエステル、キンクロラク、キンメラク、TBA(2,3,6)及びその塩並びにエステル、トリクロピル及びその塩並びにエステル、さらにはアミノシクロピラクロル及びその塩並びにエステル;
ジフルフェンゾピル、ジフルフェンゾピル−ナトリウム、ナプタラム及びナプタラム−ナトリウム;
ブロモブチド、クロルフルレノール、クロルフルレノール−メチル、シンメチリン、クミルウロン、ダラポン、ダゾメト、ジフェンゾコート、ジフェンゾコート−メチルスルファート、ジメチピン、DSMA、ジムロン、エンドタール及びその塩、エトベンザニド、フランプロプ、フランプロプ−イソプロピル、フランプロプ−メチル、フランプロプ−M−イソプロピル、フランプロプ−M−メチル、フルレノール、フルレノール−ブチル、フルルプルイミドール、ホサミン、ホサミン−アンモニウム、インダノファン、インダジフラム、マレイン酸ヒドラジド、メフルイジド、メタム、メチルアジド、メチルブロミド、メチル−ジムロン、ヨウ化メチル、MSMA、オレイン酸、オキサジクロメホン、ペラルゴン酸、ピリブチカルブ、キノクラミン、トリアジフラム、トリジファンさらには6−クロロ−3−(2−シクロプロピル−6−メチルフェノキシ)−4−ピリダジノール(CAS499223−49−3)及びその塩並びにエステル;
である。
非常に好ましいのは、定義されている式Iで表されるテトラヒドロフタルイミドと表1のそれぞれの行に定義されている物質とを唯一の除草活性化合物として含んでいる組成物であり;
最も好ましいのは、定義されている式Iで表されるテトラヒドロフタルイミドと表1のそれぞれの行に定義されている物質とを唯一の活性化合物として含んでいる組成物である。
例えば組成物1.777は、テトラヒドロフタルイミドIa18、テルブトリン(B.67)及びフェンクロラゾール(C.5)を含んでいる(表1、入力番号1.777;並びに表B、入力番号B.67及び表C、入力番号C.5を参照されたい)。
2−(2,2,7−トリフルオロ−3−オキソ−4−プロパ−2−イニル−3,4−ジヒドロ−2H−ベンゾ[1,4]オキサジン−6−イル)−4,5,6,7−テトラヒドロ−イソインドール−1,3−ジオン(Ia18)
1H NMR:δ (DMSO) 7.73 (1H, d), 7.64 (1H, d), 4.78 (2H, s), 3.34 (1H, s), 2.37 (4H, br s), 1.75 (4H, br s)。
式Iで表されるテトラヒドロフタルイミドの除草活性を以下の温室実験により実証した。
Claims (10)
- R1はハロゲンである、請求項1に記載の式Iaで表されるテトラヒドロフタルイミド。
- R3はFである、請求項1又は2に記載の式Iaで表されるテトラヒドロフタルイミド。
- R2はC3〜C6−アルキニル又はC3〜C6−ハロアルキニルである、請求項1又は2に記載の式Iaで表されるテトラヒドロフタルイミド。
- 請求項1〜4のいずれかに記載の式Iaで表される少なくとも1種のテトラヒドロフタルイミド及び少なくとも1種のさらなる活性化合物の除草活性量を含んでいる除草剤組成物。
- 除草剤B及び/又はセーフナーCの群から選ばれる2種のさらなる活性化合物を含んでいる、請求項6に記載の組成物。
- 請求項1〜4のいずれかに記載の式Iaで表される少なくとも1種のテトラヒドロフタルイミドの除草活性量又は請求項6及び7に記載の除草剤組成物と、少なくとも1種の不活性液体及び/又は固体担体と、適切であれば少なくとも1種の界面活性物質とを含んでいる除草剤組成物。
- 請求項1〜4のいずれかに記載の式Iaで表される少なくとも1種のテトラヒドロフタルイミドの除草活性量又は請求項6及び7に記載の除草剤組成物と、少なくとも1種の不活性液体及び/又は固体担体と、必要に応じて少なくとも1種の界面活性物質とを混合することを含む、除草活性組成物の調製方法。
- 請求項1〜4のいずれかに記載の式Iaで表される少なくとも1種のテトラヒドロフタルイミドの除草活性量又は請求項6及び7に記載の除草剤組成物を、植物体、その環境又は種子に作用させることを含む、望まれていない植物の防除方法。
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Publication number | Priority date | Publication date | Assignee | Title |
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EA023754B1 (ru) | 2009-06-19 | 2016-07-29 | Басф Се | Гербицидные бензоксазиноны |
DK2499136T3 (en) | 2009-11-13 | 2014-03-03 | Basf Se | 3- (3,4-dihydro-2H-benzo [1,4] oxazin-6-yl) -1H-pyrimidine-2,4-dione COMPOUNDS AS HERBICIDES |
EP2621924B1 (en) * | 2010-10-01 | 2015-03-04 | Basf Se | Herbicidal benzoxazinones |
BR112013014782A2 (pt) | 2010-12-15 | 2016-07-19 | Basf Se | composição, método para o controle de vegetação indesejada, uso de composições, método para proteger a atividade fitotóxica de uma benzoxazinona de fórmula i e método de proteção |
WO2014122674A1 (en) | 2013-02-08 | 2014-08-14 | Rallis India Limited | Process for preparation of derivatives of tetrahydrophthalimide |
CA3070195A1 (en) | 2017-07-24 | 2019-01-31 | Redag Crop Protection Ltd. | Benzoxazinone derivatives useful as herbicides |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0170191A2 (en) * | 1984-07-23 | 1986-02-05 | Sumitomo Chemical Company, Limited | Tetrahydrophtalimides, and their production and use |
JPH04501420A (ja) * | 1988-12-12 | 1992-03-12 | エフ エム シー コーポレーション | ポルフィリンの製造とその使用法 |
WO1994003454A1 (en) * | 1992-07-29 | 1994-02-17 | E.I. Du Pont De Nemours And Company | Herbicidal triazinones |
JPH06502637A (ja) * | 1990-10-18 | 1994-03-24 | モンサント・カンパニー | 除草性の置換アリール−ハロアルキルピラゾール |
US5670455A (en) * | 1992-01-29 | 1997-09-23 | E. I. Du Pont De Nemours And Company | Substituted phenylheterocyclic herbicides |
JP2000247975A (ja) * | 1999-02-25 | 2000-09-12 | Nissan Chem Ind Ltd | ヘテロ環縮合ピリミジノン誘導体及びそれらを含む除草剤 |
JP2012530098A (ja) * | 2009-06-19 | 2012-11-29 | ビーエーエスエフ ソシエタス・ヨーロピア | 除草性ベンゾオキサジノン類 |
Family Cites Families (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5304732A (en) | 1984-03-06 | 1994-04-19 | Mgi Pharma, Inc. | Herbicide resistance in plants |
BR8600161A (pt) | 1985-01-18 | 1986-09-23 | Plant Genetic Systems Nv | Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio |
EP0242236B2 (en) | 1986-03-11 | 1996-08-21 | Plant Genetic Systems N.V. | Plant cells resistant to glutamine synthetase inhibitors, made by genetic engineering |
DE3807295A1 (de) * | 1988-03-05 | 1989-09-14 | Basf Ag | Neue n-heteroaryl-tetrahydrophthalimidverbindungen |
FR2629098B1 (fr) | 1988-03-23 | 1990-08-10 | Rhone Poulenc Agrochimie | Gene chimerique de resistance herbicide |
NZ231804A (en) | 1988-12-19 | 1993-03-26 | Ciba Geigy Ag | Insecticidal toxin from leiurus quinquestriatus hebraeus |
ATE241699T1 (de) | 1989-03-24 | 2003-06-15 | Syngenta Participations Ag | Krankheitsresistente transgene pflanze |
ES2074547T3 (es) | 1989-11-07 | 1995-09-16 | Pioneer Hi Bred Int | Lectinas larvicidas, y resistencia inducida de las plantas a los insectos. |
EP0536330B1 (en) | 1990-06-25 | 2002-02-27 | Monsanto Technology LLC | Glyphosate tolerant plants |
UA48104C2 (uk) | 1991-10-04 | 2002-08-15 | Новартіс Аг | Фрагмент днк, який містить послідовність,що кодує інсектицидний протеїн, оптимізовану для кукурудзи,фрагмент днк, який забезпечує направлену бажану для серцевини стебла експресію зв'язаного з нею структурного гена в рослині, фрагмент днк, який забезпечує специфічну для пилку експресію зв`язаного з нею структурного гена в рослині, рекомбінантна молекула днк, спосіб одержання оптимізованої для кукурудзи кодуючої послідовності інсектицидного протеїну, спосіб захисту рослин кукурудзи щонайменше від однієї комахи-шкідника |
US5530195A (en) | 1994-06-10 | 1996-06-25 | Ciba-Geigy Corporation | Bacillus thuringiensis gene encoding a toxin active against insects |
DE19505995A1 (de) | 1995-02-21 | 1996-08-22 | Degussa | Verfahren zur Herstellung von Thietanonen |
WO1997041117A1 (fr) | 1996-04-26 | 1997-11-06 | Nippon Soda Co., Ltd. | Nouveaux derives du benzene substitues par des heterocycles, et herbicides |
AU1670797A (en) | 1996-04-26 | 1997-11-19 | Nippon Soda Co., Ltd. | Benzene derivatives substituted by heterocycles and herbicides |
HUP9902423A3 (en) | 1996-04-26 | 2001-02-28 | Nippon Soda Co | Benzene derivatives substituted by heterocycles and herbicides |
US5773704A (en) | 1996-04-29 | 1998-06-30 | Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | Herbicide resistant rice |
US5773702A (en) | 1996-07-17 | 1998-06-30 | Board Of Trustees Operating Michigan State University | Imidazolinone herbicide resistant sugar beet plants |
SK286030B6 (sk) | 1996-07-17 | 2008-01-07 | Michigan State University | Rastlinný materiál cukrovej repy rezistentnej voči herbicídom, spôsob produkcie herbicídne rezistentnej rastliny cukrovej repy a spôsob kontroly burín v prítomnosti týchto rastlín |
US6348643B1 (en) | 1998-10-29 | 2002-02-19 | American Cyanamid Company | DNA sequences encoding the arabidopsis acetohydroxy-acid synthase small subunit and methods of use |
AU5920601A (en) | 2000-04-28 | 2001-11-12 | American Cyanamid Co | Use of the maize x112 mutant ahas 2 gene and imidazolinone herbicides for selection of transgenic monocots, maize, rice and wheat plants resistant to the imidazolinone herbicides |
EP1226127B1 (en) | 2000-05-04 | 2009-07-01 | Basf Se | Substituted phenyl sulfamoyl carboxamides |
ES2243543T3 (es) | 2000-08-25 | 2005-12-01 | Syngenta Participations Ag | Hibridos de proteinas cristalinas de bacillus thurigiensis. |
BRPI0211809B1 (pt) | 2001-08-09 | 2019-04-24 | University Of Saskatchewan | Método para o controle de ervas daninhas nas vizinhanças de uma planta de trigo ou triticale, método para modificar a tolerância de uma planta de trigo ou triticale a um herbicida de imidazolinona e método de produção de uma planta de trigo ou triticale transgênica tendo resistência aumentada a um herbicida de imidazolinona |
US7521599B2 (en) | 2001-08-09 | 2009-04-21 | University Of Saskatchewan | Wheat plants having increased resistance to imidazolinone herbicides |
MXPA04001056A (es) | 2001-08-09 | 2005-02-17 | Northwest Plant Breeding Compa | Plantas de trigo que tienen resistencia incrementada a los herbicidas de imidazolinona. |
US7230167B2 (en) | 2001-08-31 | 2007-06-12 | Syngenta Participations Ag | Modified Cry3A toxins and nucleic acid sequences coding therefor |
AU2002361696A1 (en) | 2001-12-17 | 2003-06-30 | Syngenta Participations Ag | Novel corn event |
CA2492167C (en) | 2002-07-10 | 2015-06-16 | The Department Of Agriculture, Western Australia | Wheat plants having increased resistance to imidazolinone herbicides |
US9382526B2 (en) | 2003-05-28 | 2016-07-05 | Basf Aktiengesellschaft | Wheat plants having increased tolerance to imidazolinone herbicides |
ES2379553T3 (es) | 2003-08-29 | 2012-04-27 | Instituto Nacional De Tecnologia Agropecuaria | Plantas de arroz que tienen tolerancia aumentada a herbicidas de imidazolinona |
US8680290B2 (en) | 2004-09-03 | 2014-03-25 | Syngenta Limited | Isoxazoline derivatives and their use as herbicides |
EP1799657B1 (en) | 2004-10-05 | 2009-12-02 | Syngenta Limited | Isoxazoline derivatives and their use as herbicides |
GB0526044D0 (en) | 2005-12-21 | 2006-02-01 | Syngenta Ltd | Novel herbicides |
GB0603891D0 (en) | 2006-02-27 | 2006-04-05 | Syngenta Ltd | Novel herbicides |
GB0625598D0 (en) | 2006-12-21 | 2007-01-31 | Syngenta Ltd | Novel herbicides |
-
2010
- 2010-10-28 BR BR112012009987A patent/BR112012009987A2/pt not_active IP Right Cessation
- 2010-10-28 CN CN2010800596734A patent/CN102686583A/zh active Pending
- 2010-10-28 WO PCT/EP2010/066363 patent/WO2011051393A1/en active Application Filing
- 2010-10-28 EP EP10773899.9A patent/EP2496573B1/en not_active Not-in-force
- 2010-10-28 JP JP2012535828A patent/JP2013509379A/ja active Pending
- 2010-10-28 US US13/505,106 patent/US8445407B2/en active Active
- 2010-11-01 AR ARP100104032A patent/AR078861A1/es unknown
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0170191A2 (en) * | 1984-07-23 | 1986-02-05 | Sumitomo Chemical Company, Limited | Tetrahydrophtalimides, and their production and use |
JPH04501420A (ja) * | 1988-12-12 | 1992-03-12 | エフ エム シー コーポレーション | ポルフィリンの製造とその使用法 |
JPH06502637A (ja) * | 1990-10-18 | 1994-03-24 | モンサント・カンパニー | 除草性の置換アリール−ハロアルキルピラゾール |
US5670455A (en) * | 1992-01-29 | 1997-09-23 | E. I. Du Pont De Nemours And Company | Substituted phenylheterocyclic herbicides |
WO1994003454A1 (en) * | 1992-07-29 | 1994-02-17 | E.I. Du Pont De Nemours And Company | Herbicidal triazinones |
JP2000247975A (ja) * | 1999-02-25 | 2000-09-12 | Nissan Chem Ind Ltd | ヘテロ環縮合ピリミジノン誘導体及びそれらを含む除草剤 |
JP2012530098A (ja) * | 2009-06-19 | 2012-11-29 | ビーエーエスエフ ソシエタス・ヨーロピア | 除草性ベンゾオキサジノン類 |
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US8445407B2 (en) | 2013-05-21 |
EP2496573B1 (en) | 2015-07-01 |
EP2496573A1 (en) | 2012-09-12 |
BR112012009987A2 (pt) | 2015-09-29 |
US20120214668A1 (en) | 2012-08-23 |
CN102686583A (zh) | 2012-09-19 |
AR078861A1 (es) | 2011-12-07 |
WO2011051393A1 (en) | 2011-05-05 |
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