Organic matter – Page 5
-
Opinion
Functionalising pyridines with phosphonium salts
Newly-independent research groups often bring new perspectives to synthesis
-
Opinion
Still boiling after all these years
If you’ve got the facilities, distillation can be a powerful plant technique
-
-
-
-
Opinion
6-epi-Ophiobolin N
When it comes to cascade reactions, radicals are king of the ring-formers
-
Opinion
Lighting up crowded corners
Combining photocatalysis with organocatalysis opens doors to chiral quaternary centres
-
Opinion
Crossing the boundaries
Getting reagents across interfaces requires help from phase-transfer catalysts – but transferring information is harder
-
-
Opinion
An odd couple
Coupling unactivated phenols with amines requires an unusual approach, as Karl Collins discovers
-
Opinion
Dead in the water
A healthy sense of hydrophobia is a useful trait in the plant, says Chemjobber
-
-
Opinion
Scratching chiral surfaces
Heterogeneous asymmetric catalysis beyond hydrogenation is tricky, says Karl Collins
-
Opinion
Foaming at the reactor mouth
Turning a 1000 gallon reactor into a giant bubble bath is far from soothing, says Chemjobber
-
Opinion
Batzelladine B
Taming basic and reactive nitrogen atoms makes alkaloids more attractive targets, says BRSM
-
Opinion
A witches’ brew for trifluoromethylation
Karl Collins is surprised by the difficulty of a seemingly simple alkylation
-
Opinion
Scrubbing up
Acid vapours are problematic on scales at which they corrode cars and cause acid rain, says Chemjobber
-
Opinion
(–)-Jiadifenolide
BRSM wonders what makes a route so good it becomes the last total synthesis of a complex target
-
Opinion
Dispelling nickel’s catalytic demons
Stable Ni(IV) complexes could help nickel rival its flashier platinum-group cousins, says Karl Collins
-
Opinion
Catching the runaways
Exotherms in a plant require more than ice to avoid disaster, says Chemjobber