Mitsui Toatsu Chemicals, Incorporated

Japan Tobacco Inc.

Masatoshi Gohbara

Tsutomu Ishii

Kenichi Yamaguchi

Tatsuo Shinmi

Makoto Nishida

Satoshi Numata

Hajime Tachibana

Kiyoshi Nakatani

Takatoshi Udagawa

Tsuneo Inoue

Emi Shinmi

Tomoko Hiruta

Kazunori Takanaka

Naoki Sato

Hiroshi Tsukamoto

Kenji Kodaka

Hideo Yamazaki

Junko Watanabe

Teruhiko Toyama

Katsutoshi Ishikawa

Shuji Ozawa

Tamotsu Asano

Masanobu Arita

Yasunaga Iwasaki

Keiko Fukui

Emi Tohyama

Kengo Oda

Yutaka Kubota

Sadafumi Koda

Akira Hosono

Sunao Maeda

Tadaharu Hieda

Michiyo Takabayashi

The invention relates to a strain belonging to,which shows the esterase zymogram pattern shown in FIG.,a weed-controlling agent containing the same, and a weed-controlling method using the same. The invention provides a novel strain belonging to,excellent in herbicidal effects as well as in spore productivity.

Strain belonging to Exserohilum monoceras, and uses thereof

Waterborne microbial pesticides

Described are Drechslera monoceras var. microsporus strains, that is, new microorganism strains which show herbicidal effects against all varieties of barnyard grass, i.e., Echinochloa spp. as weed even at temperatures as low as 15.degree. C. but does not give any influence to cultivation crops such as rice; weed control compositions against barnyard grass, said compositions each containing one of the microorganism strains as an effective ingredient and having high safety and selectivity; and a barnyard grass control method employing at least one of the microorganism strains. Combined use of at least one of the microorganism strains with a chemical herbicide makes it possible to substantially reduce their dosages compared with those required when they are singly applied.

Variety of Drechslera monoceras effective for control of barnyard grass

Weed control compositions containing Drechslera monoceras and additional

Variety of Drechslera monoceras, weed control compositions containing

Described are new strains of Drechslera spp., which possess herbicidal effects against all varieties of barnyard grass, i.e., Echinochloa spp. as weed but do not give any influence to crops under cultivation such as rice. Weed control agents according to the present invention, which contain one or more of the novel strains, have high safety and selectivity, thereby providing practical control effects against barnyard grass. Weed control compositions according to the present invention, which contain one or more of the new strains in combination with one or more chemical herbicides, have sufficient herbicidal effects even at dosages which are too low to permit control of weeds when they are applied singly, thereby making it possible to reduce the dosage of herbicides. The weed control compositions can therefore contribute to the prevention of environmental pollution and the occurrence of weeds with acquired pesticide resistance.

Strains of Drechslera spp., weed control compositions containing the

Described are new strains of Drechslera spp., which possess herbicidal effects against all varieties of barnyard grass, i.e., Echinochloa spp. but do not give any influence to crops under cultivation such as rice. The control agents according to the present invention, which contain one or more of the strains, have high safety and selectivity, thereby providing practical control effects against barnyard grass. Further, the control compositions according to the present invention, which contain one or more of the new strains in combination with one or more chemical herbicides, have sufficient herbicidal effects even at dosages which are too low to permit control of barnyard grass when they are applied singly, thereby making it possible to reduce the dosage of herbicides. Thus, the control compositions can therefore contribute to the prevention of environmental pollution and the occurrence of barnyard grass with acquired pesticide resistance.

Strains of Drechslera ssp for controlling grass

Benzaldehyde acetal compounds represented by the following formula: ##STR1## in which each R is a C.sub.3-8 alkyl group and forms an ether bond with the corresponding oxygen atom of the orthoaldehyde moiety have no injury to crops and, moreover, exhibits superb herbicidal effects owing to the limitation of the number of carbon atoms of each alkyl group to 3-8.

Benzaldehyde acetal compounds, preparation process thereof, and

Herbicidally active pyridyloxypyrimidines represented by the following formula [I]: ##STR1## wherein R means a formyl group or an acetal group represented by ##STR2## R.sup.1 and R.sup.2 being the same or different and individually denoting an alkyl group having 1-4 carbon atoms or R.sup.1 and R.sup.2 being coupled together and denoting an alkylene group, R.sup.3, having 2-3 carbon atoms; are prepared by reacting 2 formyl-3-hydroxypyridine or 3-hydroxy-2-pyridine carboxaldehyde acetal with 2 halogeno-4,6 dimethoxypyrimidine in the presence of a base.

Pyridyloxypyrimidine derivatives, preparation process thereof, and

Disclosed are herbicidally active pyrimidine derivatives of the formula ##STR1## wherein R represents a hydrogen atom or an etherifying group, e.g., a lower alkyl, lower alkenyl, lower alkynyl, phenyl-substituted lower alkenyl, lower haloalkenyl, cycloalkyl, substituted phenyl-substituted lower alkenyl or phenyl-substituted lower alkynyl group; or a group represented by the following formula: ##STR2## wherein R.sup.1 represents a hydrogen atom or a lower alkyl group, X a halogen atom or a lower alkyl or lower alkoxyl group, m and n individually 0-2, and when m is 2, both Xs may be the same or different, and herbicidal compositions containing the same, alone or in combination with another herbicidally active compound, the pyrimidine derivatives being prepared by reaction of 2-(4,6-dimethoxy-2-pyrimidinyloxy)benzaldehyde with NH.sub.2 OR or with a salt of hydroxylamine followed by reaction with a halide of the formula RY wherein R has the same value as above and Y is Cl, Br or I.

Pyrimidine derivatives, preparation processes thereof, herbicide

2-(4,6-dimethoxy-2-pyrimidinyloxy)benzaldoximes, preparation processes

The present invention relates to 2-arylethyl ether or thioether derivatives represented by the following general formula [I]: ##STR1## wherein Ar stands for an aryl group, R.sup.1 stands for straight or branched chain alkyl group of 1 to 6 carbons, R.sup.2 stands for a hydrogen atom, or a methyl or ethyl group, R.sup.3 stands for a halogen atom, or a methyl or methoxyl group, R.sup.4 stands for a hydrogen or halogen atom, or a lower alkyl or lower alkoxy group, and n is an integer of 1 or 2 with the proviso that when n is 2, the groups R.sup.4 may be the same or different, and Y stands for an oxygen or sulfur atom, and also to processes for the preparation of these ethers or thioethers and a use of these ethers or thioethers. These compounds of the present invention have excellent insecticidal and acaricidal activities while the toxicity of these compounds are very low.

2-aryl-ethyl ether derivatives and insecticidal and acaricidal agents

2-Arylpropyl ether or thioether derivatives represented by the following general formula [I]: ##STR1## wherein Ar stands for an aryl group, R stands for a methyl or ethyl group, Y stands for an oxygen or sulfur atom, and B stands for a group represented by the following formula [II]: ##STR2## or the following general formula [III]: ##STR3## wherein Z stands for an oxygen or sulfur atom or a carbonyl or methylene group, R.sup.1 stands for a hydrogen or halogen atom or a lower alkyl group or a lower alkoxy group, and n is an integer of from 1 to 5 with the proviso that when n is 2 or more, the groups R.sup.1 may be the same or different, are produced by reacting a compound represented by the following formula (V): ##STR4## with a compound represented by the following formula (VI):

Process for the preparation of 2-arylpropyl ether or thioether

The present invention relates to 2-arylpropyl ether or thioether derivatives represented by the following general formula [I]: ##STR1## wherein Ar stands for an aryl group, R stands for a methyl or ethyl group, Y stands for an oxygen or sulfur atom, and B stands for a group represented by the following formula [II]: ##STR2## or the following general formula [III]: ##STR3## wherein Z stands for an oxygen or sulfur atom or a carbonyl or methylene group, R.sup.1 stands for a hydrogen or halogen atom or a lower alkyl group or a lower alkoxy group, and n is an integer of from 1 to 5 with the proviso that when n is 2 or more, the groups R.sup.1 may be the same or different, and also to processes for the preparation or these ethers of thioethers and a use of these ethers or thioethers. These compounds of the present invention have excellent insecticidal and acaricidal activities while the toxicity of these compounds are very low.

2-Arylpropyl ether or thioether derivatives and insecticidal and

Growing community of inventors

Kanagawa, Japan

Masatoshi Gohbara