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Small ring chemistry in crop protection

An overview is given of the significance of three- and four-membered rings in crop protection chemistry. The main herbicidally, fungicidally, and insecticidally active small ring derivatives are presented, together with their synthesis routes, modes of action and biological efficacies. Also the most important small ring containing natural products, which are active against weeds, insects and fungal plant diseases are covered. In addition, the role of three- and four-membered rings as intermediates in the synthesis of agrochemicals not containing such a small ring component is reported.

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Isothiazole – Wikipedia,
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BENZISOTHIAZOLES-1,2 ET -2,1: ETUDES SPECTROSCOPIQUES INFRAROUGE ET RAMAN

Infrared (4000-2000 cm-1, of vapor, liquid and solution in inert and proton-acceptor solvents) and Raman spectra (4000-100 cm-1, liquid) of 1,2- and 2,1-benzisothiazoles have been recorded.A complete assignment of the fundamental vibrations is proposed.The source of the fundamental vibrational wavenumbers is discussed for a series of benzoheterocycles: benzothiophene, 1,3-benzothiazole, benzisothiazoles and benzisoxazoles.

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Fungicides for the control of take-all disease of plants

A method of controlling Take-All disease of plants by applying a fungicide of the formula STR1 wherein Z1 and Z2 are C and are part of an aromatic ring which is benzothiophene; and A is selected from –C(X)-amine wherein the amine is an unsubstituted, monosubstituted or disubstituted amino radical, –C(O)–SR3, –NH–C(X)R4, and –C(=NR3)–XR7 ; B is –Wm –Q(R2)3 or selected from O-tolyl, 1-naphthyl, 2-naphthyl, and 9-phenanthryl, each optionally substituted with halogen or R4 ; Q is C, Si, Ge, or Sn; W is –C(R3)p H(2-p) –; or when Q is C, W is selected from –C(R3)p H(2-p), –N(R3)m H(1-m)–, –S(O)p–, and –O–; X is 0 or S; n is 0, 1, 2, or 3; m is 0 or 1; p is 0, 1, or 2; each R and R2 is independently defined herein; R3 is C1 -C4 alkyl; R4 is C1 -C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino; and R7 is C1 -C4 alkyl, haloalkyl, or phenyl, optionally substituted with halo, nitro, or R4 ; or an agronomic salt thereof.

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Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com

 

Brief introduction of 3-Piperazinobenzisothiazole hydrochloride

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Synthesis and Biological Evaluation of 1-(1,2-Benzisothiazol-3-yl)- and (1,2-Benzisoxazol-3-yl)piperazine Derivatives as Potential Antipsychotic Agents

Members of the series of title compounds were tested for potential antipsychotic activity in relevant receptor binding assays and behavioral screens.Structure-activity relationships within the series are discussed.Compound 24 (BMY 13859-1), a (1,2-benzisothiazol-3-yl)piperazine derivative, was selected for further study because of its potent and selective profile in primary CNS tests.It was active in the Sidman avoidance paradigm and blocked amphetamine-induced stereotyped behavior in dogs for up to 7 h.The compound’s lack of typical neuroleptic-like effects in therat catalepsy test and its failure to produce dopamine receptor supersensitivity following chronic administration indicate that it should not cause the movement disorders commonly associated with antipsychotic therapy.Although 24 has potent affinity for dopaminergic binding sites, its even greater affinity for serotonin receptors suggests that a serotonergic component may be relevant to its atypical profile.Compound 24 is currently undergoing clinical evaluation in schizophrenic patients.

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Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com

 

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Synthesis of some novel pyrazolo[5,1-c][1,2,4]triazine derivatives and investigation of their absorption spectra

In this study, 5-amino-4-hetarylazo-3-methyl-1H-pyrazoles were diazotised and coupled with malononitrile and ethyl cyanoacetate to give pyrazolylazo malononitriles and ethyl pyrazolylazo cyanoacetate, respectively. Ten novel pyrazolo[5,1-c][1,2,4]triazine dyes were synthesized by heating of pyrazolylazo malononitriles and ethyl pyrazolylazo cyanoacetate in glacial acetic acid. The dyes were characterized by elemental analysis and spectral methods. The solvatochromic behaviour of these diazo dyes in various solvents was evaluated. Substituent, acid and base effects on the visible absorption maxima of the dyes are also reported.

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Synthesis, fungicidal activity and SAR of 3,4-dichloroisothiazole-based cycloalkylsulfonamides

To develop more valuable and effective fungicide candidates, a novel series of 3,4-dichloroisothioxazole-based cycloalkylsulfonamides were synthesized and their structures were identified by 1H NMR, 13C NMR, MS and elemental analysis. Compound 3k was further confirmed by X-ray single crystal diffraction. The in vitro bioassay results demonstrated that the target compounds showed significant fungicidal activity on mycelial growth and spore germination of Botrytis cinerea. Especially, compound 3j, with prominent inhibition effect on mycelial with EC50 and EC80 values of 1.4 and 23.7 mug/mL respectively, was comparable to the selected commercial fungicide. Moreover, at 50 mug/mL, the inhibition rate of compound 3j on spore germination was recorded up to 89.7%. The further in vivo bioassay results indicated compound 3j continued to show high control effect on tomato leaves, flowers and fruit at 200 mug/mL, with control efficiencies of 94.3%, 89.3% and 91.9%, respectively. The structure?activity relationship showed that the compound with a five-membered ring possessed the best activity after the introduction of the active fragment of the 3,4-dichloroisothioxazole, provided a valuable idea for further creation of new fungicides.

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Isothiazole – ScienceDirect.com

 

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Orally-effective, long-acting sorbitol dehydrogenase inhibitors: Synthesis, structure – Activity relationships, and in vivo evaluations of novel heterocycle-substituted piperazino-pyrimidines

Optimization of a previously disclosed sorbitol dehydrogenase inhibitor (SDI, II) for potency and duration of action was achieved by replacing the metabolically labile N,N-dimethylsulfamoyl group with a variety of heterocycles. Specifically, this effort led to a series of novel, in vitro potent SDIs with longer serum half-lives and acceptable in vivo activity in acutely diabetic rats (e.g., 62, 67, and 69). However, the desired in vivo potency in chronically diabetic rats, ED90 ? 5 mg/kg/day, was achieved only through further modification of the piperazine linker. Several members of this family, including 86, showed better than the targeted potency with ED90 values of 1-2 mg/kg/day. Compound 86 was further profiled and found to be a selective inhibitor of sorbitol dehydrogenase, with excellent pharmacodynamic/pharmacokinetic properties, demonstrating normalization of sciatic nerve fructose in a chronically diabetic rat model for ?17 h, when administered orally at a single dose of 2 mg/kg/day.

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Isothiazole – Wikipedia,
Isothiazole – ScienceDirect.com

 

Discovery of Benzo[d]isothiazole

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Complete study of the pyrolysis and gasification of scrap tires in a pilot plant reactor

The pyrolysis and gasification of tires was investigated in a pilot plant reactor provided with a system for condensation of semivolatile matter. The study comprised experiments at 450, 750, and 1000C both in nitrogen and 10% oxygen atmospheres. In the gas phase, only methane and benzene yields increased with temperature until 1000C. In the liquids, the main components were styrene, limonene, and isoprene. The solid fraction (including soot) increased with temperature. Zinc content of the char decreased with increasing temperature. Analysis of the surface area of the solids showed that the area was similar in all cases to that of a commercial carbon black. The higher surface of the soot with respect to the chars was observed. The results coincided with published findings, i.e., kinetic severity function values would produce 0.2% of methane at 450C and 4.5% at 750-1000C.

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4,6-Dinitrobenzo[c]isothiazole: Synthesis and 1,3-dipolar cycloaddition to azomethine ylide

1,3-Dipolar cycloaddition of 4,6-dinitrobenzo[c]isothiazole to (N-methyl-N-methylideneammonio)methanide (2 equiv.) gives 5,8-dimethyl-3b,6b- dinitrodecahydroisothiazolo[3,4-e]pyrrolo[3,4-g]isoindole, whose structure was confirmed by X-ray diffraction analysis.

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Imidazo[1,2-a]pyridines: Promising drug candidate for antitumor therapy

Imidazo[1,2-a]pyridine has been shown to be an important biologically active moiety. This review is a compilation of the scattered output of results of the anticancer activities of the imidazo[ 1,2-a]pyridine system since 2001, which have been classified as inhibition of CDK, VEGFR, PI3K, EGFR, RGGT etc. along with inhibition against different tumor cell lines. Various imidazo[ 1,2-a]pyridine based analogues have been used as lead molecules and are now under human clinical trials. This review will help the wider scientific community in the area of drug discovery of imidazo[1,2-a]pyridines as novel anticancer agents.

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