Discovery of Novel Antimicrobial-Active Compounds and Their Analogues by In Silico Small Chemical Screening Targeting <i>Staphylococcus aureus</i> MurB. [PDF]
Okubo S, Hirose S, Aoki S.
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Decoding mEos4b day-long maturation and engineering fast-maturing variants. [PDF]
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Lighting Up Endogenous RNA: Fluorescent Aptamer Sensors for Live-Cell Imaging. [PDF]
Ma Z, Kulsoom, Wang F.
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Occurrence of insecticides, fungicides, and herbicides in household drinking and irrigation water in an intensive floriculture region of Ecuador. [PDF]
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Structure-based insights into fluorogenic RNA aptamers. [PDF]
Song Q, Tai X, Ren Q, Ren A.
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2-Imidazolinones were synthesized by heating α-bromoketones with urea in ethyleneglycol in the presence of potassium carbonate.
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Copper(II) complexes of imidazolinone herbicides
Inorganica Chimica Acta, 1997Abstract The copper(II) complexes formed by the imidazolinone herbicide Imazapyr or (±)-2-4-isopropyl-(4-methyl-5-oxo-2-imidazolin-2-yl)-nicotinic acid (H 2 imz) are described. The compounds isolated in the solid state confirm that Imazapyr is a versatile bipy-like ligand able to chelate the metal ion through two different donor sets.
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Palladium-Catalyzed Direct Functionalization of Imidazolinone: Synthesis of Dibromophakellstatin [PDF]
The direct C−H functionalization of imidazolinone is achieved with Pd(OAc)2/NaOAc in DMSO. Dibromophakellstatin can be synthesized in five steps with 40% overall yield using this new C−H activation method.
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The asymmetric reduction of imidazolinones with trichlorosilane
Chemical Communications, 2017The asymmetric reduction of imidazolinones with trichlorosilane is described, catalyzed through a chiral bispyrrolidine organocatalyst.
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Abstract A field study was performed in imidazolinone-resistant maize in order to evaluate the effectiveness and carryover effect on rotational crops of two formulated mixtures of imidazolinone herbicides: imazapyr plus imazapic and imazapyr plus imazethapyr.
Alister, C, Kogan, M
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