Abstract
The metal-promoted nucleophilic addition of sulfur ylides to π-systems is a well-established reactivity. However, the driving force of such transformations, elimination of a sulfide moiety, entails stoichiometric byproducts making them unfavorable in terms of atom economy. In this work, a new take on sulfur ylide chemistry is reported, an atom-economical gold(I)-catalyzed synthesis of dihydrobenzo[b]thiepines. The reaction proceeds under mild conditions at room temperature.
Author supplied keywords
Cite
CITATION STYLE
Knittl-Frank, C., Saridakis, I., Stephens, T., Gomes, R., Neuhaus, J., Misale, A., … Maulide, N. (2020). Gold-Catalyzed Cycloisomerization of Sulfur Ylides to Dihydrobenzothiepines. Chemistry - A European Journal, 26(48), 10972–10975. https://doi.org/10.1002/chem.202000622
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.