Abstract
We demonstrate that aryltriazenes can promote three distinctive types of C-H functionalization reactions, allowing the preparation of complex benzene molecules with diverse substitution patterns. 2-Triazenylbenzaldehydes are shown to be efficient substrates for Rh(I)-catalyzed intermolecular alkyne hydroacylation reactions. The resulting triazene-substituted ketone products can then undergo either a Rh(III)-catalyzed C-H activation, or an electrophilic aromatic substitution reaction, achieving multifunctionalization of the benzene core. Subsequent triazene derivatization provides traceless products.
Original language | English |
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Pages (from-to) | 6091-6098 |
Number of pages | 8 |
Journal | ACS Catalysis |
Volume | 11 |
Issue number | 10 |
DOIs | |
State | Published - 21 May 2021 |
Bibliographical note
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Keywords
- benzene
- hydroacylation
- rhodium
- sequential catalysis
- triazene