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a few cases (specifically stated in the experimental) all purifications were carried out on<br />

2cm diameter columns collecting 50 ml fractions. Where 3cm <strong>and</strong> 1cm columns were<br />

used, 100 ml fractions <strong>and</strong> 10 ml fractions were collected respectively. Any deviations to<br />

these conditions are mentioned specifically in the experimental.<br />

Infrared Spectroscopy (IR Spectroscopy)<br />

Infrared spectra were recorded on a PerkinElmer TM Spectrum 100. The sample was<br />

dissolved in either dichloromethane or methanol before being loaded onto the surface <strong>of</strong><br />

potassium bromide discs.<br />

Ultraviolet Absorption Spectroscopy (UV)<br />

Ultraviolet absorption spectra were recorded with a PerkinElmer TM Lambda 35 UV/VIS<br />

spectrophotometer. Samples were dissolved in either dichloromethane or methanol <strong>and</strong><br />

made to concentrations between 0.0052g/100ml <strong>and</strong> 1.2g/100ml.<br />

Optical Rotation<br />

Optical rotations were performed with a PerkinElmer TM , Model 341 Polarimeter. The<br />

samples were dissolved in dichloromethane or methanol <strong>and</strong> were measured at room<br />

temperature. Concentrations were calculated in g/100mL.<br />

Gas Chromatography-Mass Spectrometry (GC-MS)<br />

The mass spectra were registered on an Agilent MS 5973 instrument which was coupled<br />

to an Agilent GC 6890 instrument equipped with a DB-5MS (30m x 0.25 id, 0.25 µm<br />

stationary phase) column. Helium (at 0.7ml/min) was used as the carrier gas. Optimal<br />

results required that the oven temperature be maintained at 200 o C for one minute<br />

followed by 5<br />

98<br />

o C increments in temperature every minute until an oven temperature <strong>of</strong>

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