Structure Determination and Synthesis of Fluoro Nissl Green: An RNA-Binding Fluorochrome

Merlic, Craig A.; Motamed, Soheil; Quinn, Bruce

doi:10.1021/jo00116a020

Cited by 80 publications

(28 citation statements)

References 1 publication

(4 reference statements)

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“…Sithambaram reported direct catalytic synthesis of imines from alcohols using manganese octahedral molecular sieves [35], Taylor described a tandem oxidation-imine formation process from alcohols with active manganese oxide [36,37], Korich developed a facile, one pot procedure to afford diarylimines [38], Macho reported one stage preparation of Schiff's bases from nitroarenes, aldehydes and carbon monoxide in the presence of water [39], tandem nitroarene reduction and intramolecular Schiff base condensation to provide heteroarenes has also been reported [40,41].…”

Section: Introductionmentioning

confidence: 99%

One Pot Synthesis of Imines from Aromatic Nitro Compounds with a Novel Ni/SiO2 Magnetic Catalyst

Zheng

et al. 2008

Catal Lett

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We have successfully prepared a novel Ni/SiO 2 magnetic catalyst, and put it into the process of one pot synthesis of imines directly from aromatic nitro compounds and aldehydes for the first time. The catalyst has been characterized by XRD, IR, TEM, SEM, TPR, H 2 -TPD and XPS. The prominent merits of the Ni/SiO 2 magnetic catalyst passivated with a gas mixture are that it can be stored safely in air below 423 K and needs no activation before use. In the catalytic test, most conversion and selectivity is almost up to 100%, and it is found that the catalyst is highly efficient, stable, and reusable for the synthesis of imines.

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Section: Introductionmentioning

confidence: 99%

One Pot Synthesis of Imines from Aromatic Nitro Compounds with a Novel Ni/SiO2 Magnetic Catalyst

Zheng

et al. 2008

Catal Lett

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“…The organic phases were combined and washed with water (100 mL×2) and brine (100 mL), and dried over sodium sulfate. Upon removal of the solvent, the resulting residue was subjected to column chromatography (petroleum ether/ AcOEt/NEt 3 , V∶V∶V＝100∶100∶1) to give compound 3 13 as a yellow solid (1.80 g, 87%). 1 9 mmol) in acetone (25 mL) was stirred at 60 ℃ for 12 h and then concentrated with a rotary evaporator.…”

Section: Compoundmentioning

confidence: 99%

Self‐Assembly of Vesicles by a 2,6‐Di(7‐benzamidy)quinolin‐2‐ yl)pyridine Derivative Tuned by an Amphiphilic Amide Chain

You

Zhao

2010

Chin. J. Chem.

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This paper describes 2-(2-(dioctylamino)-2-oxoethyl-amino)-2-oxoethoxyl (DOAOE)-tuned self-assembly of vesicles from a 2,6-di(7-benzamidy)-quinolin-2-yl)pyridine derivative. Scanning electron (SEM), transmission electron (TEM) and optical microscopy and dynamic light scattering (DLS) studies reveal that the molecule self-assembles into vesicular structures in methanol. The influence of the transition metal ions and trifluoroacetic acid on the formation of the vesicles was investigated. The results illustrate that DOAOE is robust in promoting the formation of vesicles for aromatic systems in polar medium.

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“…Anilines are an important class of precursors for the synthesis of pharmaceuticals, dyes, and other biologically active compounds such as Glu-P-1 and Trp-P-2, [3][4][5] and can be produced by selective reduction of nitroaromatic compounds. While traditional methods such as reduction with iron powder in presence of hydrochloric or acetic acid 6 are gradually being eliminated due to environmental issues, catalytic hydrogenation processes have emerged as more effective alternatives. Some of the recent reports in this context include application of silver nanoparticles stabilized by polyaminocyclodextrin, and Pd/Fe bimetal nanoparticles embedded in P-doped mesoporous carbons, 19 have also been reported.…”

Section: Introductionmentioning

confidence: 99%

A highly effective Ag–RANEY® nickel hybrid catalyst for reduction of nitrofurazone and aromatic nitro compounds in aqueous solution

Khorshidi

Ghorbannezhad

2017

RSC Adv.

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RANEY® nickel reduced Ag+ ions to form ultrafine spherical silver nanoparticles over itself, and the obtained hybrid material was used as catalyst for efficient and selective reduction of aromatic nitro compounds, and nitrofurazone as a non-aromatic example, in aqueous solution by using NaBH 4 as reducing agent. Other silver nanostructures with different morphologies such as silver nano-flowers were also prepared and their efficiency in the reduction process was evaluated. Ag-RANEY® nickel catalyst however, had superior advantages including mild reaction conditions, higher conversion yield, and reduction in aqueous solution at near ambient temperature. The catalyst was also recoverable and showed 5% decrease in efficiency after six successive runs.

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Structure Determination and Synthesis of Fluoro Nissl Green: An RNA-Binding Fluorochrome

Cited by 80 publications

References 1 publication

One Pot Synthesis of Imines from Aromatic Nitro Compounds with a Novel Ni/SiO2 Magnetic Catalyst

One Pot Synthesis of Imines from Aromatic Nitro Compounds with a Novel Ni/SiO2 Magnetic Catalyst

Self‐Assembly of Vesicles by a 2,6‐Di(7‐benzamidy)quinolin‐2‐ yl)pyridine Derivative Tuned by an Amphiphilic Amide Chain

A highly effective Ag–RANEY® nickel hybrid catalyst for reduction of nitrofurazone and aromatic nitro compounds in aqueous solution

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