The present invention provides a method for controlling a soybean rust fungus having an amino acid substitution of F129L on mitochondrial cytochrome b protein, by applying a compound represented by formula (I) [wherein Q represents a group represented by the following Q1, Q2, Q3, Q4 or Q5 (in the formulae, .circle-solid. represents a binding site to benzene ring); X represents an oxygen atom or NH; L represents CH.sub.2, an oxygen atom or NCH.sub.3; E represents a C6-C10 aryl group, etc.; R.sup.1 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R.sup.2 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R.sup.3 represents a C1-C3 alkoxy group or a C1-C3 chain hydrocarbon group, etc.; and n is 0, 1, 2, or 3] or its N oxide or an agriculturally acceptable salt thereof.

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A lithium air secondary battery is allowed to operate as a high-capacity secondary battery, thereby implementing high output and a large discharge capacity. A lithium air secondary battery 100 includes an air electrode 102 using oxygen in the air as a positive electrode active material, a negative electrode 104 using metallic lithium or a lithium-containing material as a negative electrode active material, and an organic electrolyte 106 placed between the air electrode 102 and the negative electrode 104, and including a lithium salt. The organic electrolyte 106 includes a crown ether compound having an azo group as an additive.

A lithium air secondary battery is allowed to operate as a high-capacity secondary battery, thereby implementing high output and a large discharge capacity. A lithium air secondary battery 100 includes an air electrode 102 using oxygen in the air as a positive electrode active material, a negative electrode 104 using metallic lithium or a lithium-containing material as a negative electrode active material, and an organic electrolyte 106 placed between the air electrode 102 and the negative electrode 104, and including a lithium salt. The organic electrolyte 106 includes a crown ether compound having an azo group as an additive.

The present invention relates to a method for producing a lactam compound from dioxazolone in the presence of a catalyst having a particular ligand, and to a lactam compound produced thereby, and can produce a lactam compound with excellent selectivity and an excellent yield by using the combination of a starting material having a particular functional group and a particular catalyst having a particular ligand.

The present invention relates to a method for producing a lactam compound from dioxazolone in the presence of a catalyst having a particular ligand, and to a lactam compound produced thereby, and can produce a lactam compound with excellent selectivity and an excellent yield by using the combination of a starting material having a particular functional group and a particular catalyst having a particular ligand.

Chemoselective conjugation is achieved through redox reactivity by reacting an N-transfer oxidant with a thioether substrate in a redox reaction in an aqueous environment to form a conjugation product. In embodiments, Redox-Activated Chemical Tagging (ReACT) strategies for methionine-based protein functionalization. Oxaziridine (Ox) compounds serve as oxidant-mediated reagents for direct functionalization by converting methionine to the corresponding sulfimide conjugation product.

The invention relates to the use of compounds according to general formula (1), in particular 1,4,2-dioxoazol-5-on-derivatives, as additives in electrolytes for electrochemical energy sources such as lithium-ion-batteries, and compounds containing electrolytes according to general formula (1), in particular 1,4,2-dioxoazol-5-on-derivatives.

The invention relates to the use of compounds according to general formula (1), in particular 1,4,2-dioxoazol-5-on-derivatives, as additives in electrolytes for electrochemical energy sources such as lithium-ion-batteries, and compounds containing electrolytes according to general formula (1), in particular 1,4,2-dioxoazol-5-on-derivatives.

The present disclosure relates to 1,3,5-dioxazine derivatives of formula (I) capable of reducing or eliminating hydrogen sulfide and other objectionable sulfides from oil field produced hydrocarbon fluids such as petroleum, fuel oil, gasoline, diesel, liquid propane, liquid butane, an aquaculture and production/processing of syngas/natural gas. The present disclosure further provides a method for preparing 1,3,5-dioxazine derivatives of formula I, and a method for scavenging sulfur-based species including, but not limited to hydrogen sulfide or alkyl/aryl mercaptans from a medium.

The present disclosure relates to 1,3,5-dioxazine derivatives of formula (I) capable of reducing or eliminating hydrogen sulfide and other objectionable sulfides from oil field produced hydrocarbon fluids such as petroleum, fuel oil, gasoline, diesel, liquid propane, liquid butane, an aquaculture and production/processing of syngas/natural gas. The present disclosure further provides a method for preparing 1,3,5-dioxazine derivatives of formula I, and a method for scavenging sulfur-based species including, but not limited to hydrogen sulfide or alkyl/aryl mercaptans from a medium.