| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5213879 | Tetrahedron | 2016 | 8 Pages |
Abstract
The combination of ring closing, or enyne metathesis with oxidation in order to prepare N-sulfonyl pyrroles is described. Reasonable to good yields were obtained for a variety of substituents and the procedure may also be conducted in one-pot. 2-Bromo N-sulfonyl adducts prepared in this manner were subjected to an intramolecular Heck-type cyclisation, forming cyclic sulfonamides.
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