Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. , Application In Synthesis of trans-Cyclohexane-1,2-diamine, 1121-22-8, Name is trans-Cyclohexane-1,2-diamine, molecular formula is C6H14N2, belongs to chiral-catalyst compound. In a document, author is Kikuchi, Jun, introduce the new discover.
An enantioselective [4 + 2] cycloaddition reaction of a-fluorostyrenes with N-benzoyl imines was demonstrated using a chiral phosphoric acid catalyst. Cycloaddition products having fluorine functionality were formed in high yields with excellent diastereo- and enantioselectivities. Further manipulation of the enantioenriched cycloaddition product with silyl enol ether in the presence of BiCl3 catalyst afforded substitution product with retention of the dihydro-4H-1,3-oxazine framework through selective carbon-fluorine bond cleavage without loss of enantiomeric excess.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 1121-22-8. Application In Synthesis of trans-Cyclohexane-1,2-diamine.
Reference:
Chiral Catalysts,
,Chiral catalysts – SlideShare