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Now You See Me, Now You Don’t- a Judicious Work-Around for Over-Bromination at Benzylic Carbon

One of the most challenging reactions we carry out as synthetic chemists is bromination of a benzylic carbon- the so called Wohl-Ziegler reaction.1 It’s a seemingly simple transformation – not particularly difficult to perform- and potentially very useful. In fact it’s a little too easy. Just add NBS and a radical initiator to an aryl

Using Electrochemistry to Make Carbon-Carbon Bond Formation More Sustainable

Finding generally applicable, more sustainable, scalable methods to construct C-C bonds via cross-coupling is likely to be one of the major challenges that process chemists will face over the next decade. At the moment chemists overwhelmingly rely on pre-formed nucleophilic organometallics (such as Grignard, organozinc and organoboron reagents) in C-C couplings with an electrophile (such

Accelerating Reaction Development through Open-Source HPLC Data Analysis

Acquisition and processing of analytical HPLC data is often the main bottleneck when performing automated data-rich or high-throughput experimentation. Even though it was over 20 years ago, I well remember spending most of each day running, processing and compiling HPLC data when using an automated reaction platform to run 4 data-rich time course experiments in

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