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3 protocols using dionex rslc

1

Analytical Characterization of Compounds

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All PCR reactions were carried out on a C1000 thermal cycler (BioRad). DNA sequencing was performed by Elim BioPharm Inc. Preparative scale reverse-phase analytical and semipreparative HPLC was performed using a Dionex UHPLC with a photo-diode array UV/Vis detector (Thermo Fisher Scientific). HRMS analysis was conducted using a Q Exactive Benchtop Quadrupole-Orbitrap mass spectrometer (Thermo Fisher Scientific) equipped with a Dionex RSLC (Thermo Fisher Scientific). Conventional low-resolution LC-MS analysis was conducted with a Shimadzu LCMS-2020 system. The NMR spectrum was recorded on a Bruker AV600 (600 MHz) spectrometer or a Bruker Avance III 700 MHz spectrometer equipped with a 1H/13C/15N triple-resonance inverse probe (1.7 mm microprobe).
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2

Analytical Characterization of Compounds

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All PCR reactions were carried out on a C1000 thermal cycler (BioRad). DNA sequencing was performed by Elim BioPharm Inc. Preparative scale reverse-phase analytical and semipreparative HPLC was performed using a Dionex UHPLC with a photo-diode array UV/Vis detector (Thermo Fisher Scientific). HRMS analysis was conducted using a Q Exactive Benchtop Quadrupole-Orbitrap mass spectrometer (Thermo Fisher Scientific) equipped with a Dionex RSLC (Thermo Fisher Scientific). Conventional low-resolution LC-MS analysis was conducted with a Shimadzu LCMS-2020 system. The NMR spectrum was recorded on a Bruker AV600 (600 MHz) spectrometer or a Bruker Avance III 700 MHz spectrometer equipped with a 1H/13C/15N triple-resonance inverse probe (1.7 mm microprobe).
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3

NMR and Mass Spectrometric Analysis

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NMR spectra were obtained on a Bruker Ascend 500 MHz spectrometer equipped with a cryoprobe (Bruker Biospin GmbH, Waldbronn, Germany), in the solvents indicated and referenced to residual 1 H signals in deuterated solvents. ESI-MS were acquired using an Agilent 1100 Series (Agilent Technologies, Waldbronn, Germany) separations module equipped with an Agilent 1100 Series LC/MSD mass detector in both positive and negative ion modes under the following conditions: Zorbax C 8 column, 150 × 4.6 mm, eluting with 95% H 2 O/MeCN to 5% H 2 O/MeCN (with isocratic 0.01% TFA) over 22 min at 0.4 ml min -1 and then held for 5 min. HRMS was carried out using an UltiMate 3000 rapid separation liquid chromatography system (Dionex RSLC, Thermo Fisher Scientific, Dreieich, Germany) coupled to an UHR-TOF mass spectrometer (Bruker Daltonik MaXis, Bruker Daltonik GmbH, Bremen, Germany) operating in the positive ESI mode.
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