Abstract
Pd-catalyzed arylation or benzylation of nitroazoles using aryl sulfonates or benzyl acetates is described. Electronically varied aryl tosylates and mesylates, as well as benzyl acetates, afford the arylated and benzylated products. Arylation of nitrobenzene is also reported. The relative rate for the arylation of halides is greater than that of tosylates using the reported reaction parameters. These studies enhance the scope of electrophiles for nitroarene arylations and benzylations, which was hitherto limited to the use of halide electrophiles.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 6946-6957 |
| Number of pages | 12 |
| Journal | Journal of Organic Chemistry |
| Volume | 82 |
| Issue number | 13 |
| DOIs | |
| State | Published - Jul 7 2017 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2017 American Chemical Society.
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