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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