All Organic matter articles – Page 6
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Opinion
Scratching chiral surfaces
Heterogeneous asymmetric catalysis beyond hydrogenation is tricky, says Karl Collins
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Opinion
Foaming at the reactor mouth
Turning a 1000 gallon reactor into a giant bubble bath is far from soothing, says Chemjobber
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Batzelladine B
Taming basic and reactive nitrogen atoms makes alkaloids more attractive targets, says BRSM
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A witches’ brew for trifluoromethylation
Karl Collins is surprised by the difficulty of a seemingly simple alkylation
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Scrubbing up
Acid vapours are problematic on scales at which they corrode cars and cause acid rain, says Chemjobber
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(–)-Jiadifenolide
BRSM wonders what makes a route so good it becomes the last total synthesis of a complex target
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Dispelling nickel’s catalytic demons
Stable Ni(IV) complexes could help nickel rival its flashier platinum-group cousins, says Karl Collins
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Catching the runaways
Exotherms in a plant require more than ice to avoid disaster, says Chemjobber
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Limaspermidine and deethylibophyllidine
Desymmetrisation offers a neat way to add tricky features, says BRSM
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Back to basics for silylation
Karl Collins applauds the simplicity of adding silicon to heterocycles with KOtBu
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Enthralled by evaporation
A giant rotary evaporator is a mesmerising thing, says Chemjobber, but the plant requires a different approach
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Rubriflordilactone A
Sometimes it’s worth building aromatics instead of buying them, says BRSM
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Alkynes reverse reactivity
A mild coupling of alkynes with thiol nucleophiles appeals to Karl Collins
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Synthesising the midnight oil
A chemical plant on a night shift is just as lively as through the day, says Chemjobber, but for different reasons
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Lycopodium alkaloids
Not all natural products are created equal. BRSM looks at a flexible route to some perennial favourites
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Twisting activity from amides
When amides get out of shape, a whole new world of asymmetric aldol reactions opens up, says Karl Collins
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Trekking across chemical frontiers
You can’t shake a 1000 gallon reactor, says Chemjobber, so plant-scale hydrogenation is a challenge of phase boundaries
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Psylloborine A
Late stage dimerisation is a tantalisingly elegant but risky strategy for total synthesis, says BRSM
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Opinion
Show the way but leave no trace
Karl Collins examines a stealthy strategy for directed C–H activation