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| Scientists have discovered a new way of making specific versions of asymmetrical chemicals. Photo Credit: Michal Jarmoluk |
New research from the University of Bath and the University of St Andrews, published in Nature Chemistry, has discovered the key to unlocking an 80-year-old chemical puzzle, which could have important ramifications for fine chemical processes like those involved in the manufacture of medicines.
Chiral molecules are asymmetric or non-superimposable on their mirror image – each side is different, existing in “right hand” and “left hand” forms. Often only one of these “handed” forms has the desired chemical or biological activity, while the other may have unwanted side effects.
Using a combination of lab experiments and quantum chemistry calculations, researchers have now discovered a new way to control the handedness of a notoriously difficult chemical process, known as the ‘[1,2]-Wittig rearrangement’ that will impact on how scientists design selective chemical reactions.




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