The researchers found that transient formation of hydrogen bonding between a substrate and the catalyst induced such high segregation in the reaction. By using inexpensive and readily available feedstock hydrocarbons, the researchers produced a group of chiral lactams in different shapes. Their diverse structures allow lactams to correspond to different pharmaceutical drugs.
from Top Technology News -- ScienceDaily https://www.sciencedaily.com/releases/2019/02/190221110520.htm
from Top Technology News -- ScienceDaily https://www.sciencedaily.com/releases/2019/02/190221110520.htm
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