In theory, shining the right wavelength of
 light onto carbon-carbon double bonds should pair them up into 
four-membered cyclobutane
                     rings. In practice, however, this route can prove 
finicky and inefficient, particularly if the necessary wavelength lies 
deep
                     in the ultraviolet region. Hoyt et al. 
report an iron catalyst that coaxes a wide variety of simple olefins 
into such rings without the need for photoexcitation
                     (see the Perspective by Smith and Baran). 
Systematic optimization of the ligand coordinated to iron effectively 
eliminated
                     competing pathways to alternative products.
                  Jake Yeston
 
 
 
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