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400 mr ddr2

Manufactured by Agilent Technologies

The 400-MR DDR2 is a lab equipment product from Agilent Technologies. It is a memory module that supports DDR2 (Double Data Rate 2) technology.

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2 protocols using 400 mr ddr2

1

NMR and Mass Spectrometry Characterization

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NMR spectra were recorded on Varian Mercury
Plus 300 (299.97 MHz for 1H, 75.44 MHz for 13C, and 282.23 MHz for 19F) or Agilent 400-MR DDR2 (399.94
MHz for 1H, 100.58 MHz for 13C, and 376.29 MHz
for 19F) at 298 K unless otherwise indicated. Chemical
shifts δ are given in parts per million, using residual solvent
as an internal standard. 19F NMR and 31P NMR
chemical shifts were measured relative to CCl3F and H3PO4, respectively. Coupling constants J are reported in hertz. High-resolution mass spectra were obtained
on Q-Tof Micro (Waters), equipped with a quadrupole, TOF analyzers,
and an MCP detector or LTQ Orbitrap Velos (Thermo Fisher Scientific).
Gas chromatography–mass spectrometry (GC–MS) spectra
were obtained on GC–MS DSQ II (Thermo). Thin layer chromatography
analyses were carried out on DC Alufolien Kieselgel 60 F254 (Merck).
Preparative column chromatography separations were performed on silica
gel Kieselgel 60 of 0.040–0.063 mm (Merck). Melting points
were measured on a Boetius melting point apparatus and are uncorrected.
Starting materials, reagents, and substrates were obtained from commercial
suppliers and used without further purification. The solvents were
purified and dried using standard procedures. For synthesis of reagents,
see the Supporting Information.
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2

Synthesis and Purification of Organic Compounds

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Chemicals used for the synthesis were obtained from commercial sources (Sigma Aldrich, St. Louis, MO, USA and Acros Organics, Geel, Belgium). Hexane, DCM, and EtOAc were acquired from commercial sources and were used after distillation. Molecular sieves were used to dry solvents denoted as dry. Other commercial reagents and solvents were used without further purification. The reactions were monitored with the aid of thin-layer chromatography (TLC Silica gel 60 F254) and pre-coated reverse-phase gel plates (TLC RP-18 F254). All operations involving air-sensitive reagents were performed under an inert atmosphere of dry argon and dried solvents. Melting points were determined using a melting point apparatus (PGH Rundfunk-Fernsehen, Niederdorf, Germany), and they are uncorrected. NMR spectroscopy was performed in CD3OD or DMSO at room temperature using a Varian Gemini 300 MHz (1H NMR 300 MHz, 13C NMR 75 MHz) and an Agilent 400 MR DDR2 (1H NMR 400 MHz, 13C NMR 100 MHz). Preparative HPLC was performed using COMBIFLASH RF200 UV/VIS (Teledyne ISCO, Lincoln, NE, USA). An in-house made column was prepared by filling a cartridge with polar silica (Merck, Darmstadt, Germany) for normal phase HPLC. For reverse phase HPLC, the commercially available RediSep® Gold C18 column (Teledyne ISCO) was used.
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