Abstract
The intramolecular cross-coupling of sulfonic acid derivatives occurs in the presence of tris(trimethylsilyl)silane (TTMSS) at room temperature and in air to form biaryl compounds. A photoredox-catalyzed procedure is also described. These protocols provide mild and convenient alternatives to standard tin-mediated reactions. Combined with the trivial preparation of the substrates from activated sulfonic acids and 2-halophenols or anilines, this work presents a useful means to employ sulfonic acid derivatives in cross-coupling transformations. A modified linker to realize high regioselectivity is also presented. Finally, a one-pot cross-coupling procedure is demonstrated.
Original language | English (US) |
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Pages (from-to) | 64-69 |
Number of pages | 6 |
Journal | Organic Chemistry Frontiers |
Volume | 5 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2018 |
All Science Journal Classification (ASJC) codes
- Organic Chemistry