60148-63-2Relevant articles and documents
PYRETHROID COMPOUND, AND HAIR RESTORER AND HAIR RESTORER COMPOSITION COMPRISING THE SAME
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Paragraph 0028; 0029, (2017/08/26)
PROBLEM TO BE SOLVED: To provide a pyrethroid compound having hair growth effect. SOLUTION: The present invention provides a pyrethroid compound represented by general formula (1) [in general formula (1), R1 is selected from a hydrogen atom, a halogen atom, an azido group, an alkoxy group having 1 to 4 carbon atoms, and an alkyl group having 1 to 4 carbon atoms, R2 is selected from a methyl group, an ethyl group and an isopropyl group, R3 is selected from -C≡N, -C≡CH, -C≡C-CH3 and -CH=CH2, and R4 is selected from a methyl group, a phenyl group, a 2-methoxy ethyl group, a methoxymethyl group, and a propargyl group]. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT
A facile synthesis of α-fluoro ketones catalyzed by [Cp*IrCl2]2
Ahlsten, Nanna,Bartoszewicz, Agnieszka,Agrawal, Santosh,Martin-Matute, Belen
supporting information; experimental part, p. 2600 - 2608 (2011/10/02)
Allylic alcohols are isomerized into enolates (enols) by [Cp*IrCl2]2. The enolates react with Selectfluor present in the reaction media. This method produces α-fluoro ketones as single constitutional isomers in high yields. Georg Thieme Verlag Stuttgart. New York.
Building molecular complexity via tandem ru-catalyzed isomerization/C-H activation
Bartoszewicz, Agnieszka,Martin-Matute, Belen
supporting information; experimental part, p. 1749 - 1752 (2009/09/06)
A tandem isomerization/C-H activation of a My lie alcohols was performed using a catalytic amount of RuCI2(PPh3)3. A variety of ortho alkylated ketones have been obtained in excellent yields. This tandem process relies on an in situ generation of a carbonyl functional group that directs the ortho C-H bond activation.
Process for the preparation of insecticidally active diphenylether compounds
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, (2008/06/13)
This invention relates to a process for the preparation of insecticidally active compounds and to novel styrene derivatives useful as intermediates therein.
Insecticidal benzylfurylmethyl esters of 3-(2,2-dichlorovinyl)-2,2-dimethyl-cyclopropane carboxylic acids
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, (2008/06/13)
Novel carboxylic acid esters of the formula STR1 where R1, R2 and R3 are identical or different and each is hydrogen, halogen or alkyl or alkenyl of up to 5 carbon atoms, Y is 3-(2,2-dihalogenovinyl)-2,2-dimethyl-cycloprop
Vinylcyclopropanecarboxylic acid-3-phenoxy-α-vinylbenzyl esters, processes for producing them, and their use in combating pests
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, (2008/06/13)
Vinylcyclopropanecarboxylic acid-3-phenoxy-α-vinylbenzyl esters of the formula STR1 in which X1 is fluorine, chlorine or bromine, X2 is hydrogen or bromine, and Y is hydrogen or methyl, processes for producing them, and their use in
Cyclopropanecarboxylic acid-phenoxy-α-vinyl-benzyl esters, processes for producing them, and their use in combating pests
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, (2008/06/13)
Cyclopropanecarboxylic acid-phenoxy-α-vinyl-benzyl esters of the formula STR1 in which Y is chlorine or bromine, and R1 is --CH=CH2 or STR2 processes for producing them, and their use in combating pests.