Abstract
The discovery of the copper-promoted Chan-Lam coupling
reaction with boronic acids more than ten years ago has greatly
advanced the carbon-heteroatom cross-coupling chemistry.
The N-arylation/O-arylation methodology is now a powerful
new synthetic tool, made even more attractive by the mild conditions
required. Significant progress has been made in expanding the scope and
the applications as well as understanding the mechanism of this reaction.
This review includes an examination of various C-X cross-couplings
using boronic acids and their derivatives, and a survey of the mechanistic
studies that have been carried out.
1 General Introduction
2 C-N Cross-Coupling
2.1 Original NH-Containing Substrates
2.2 Factor Xa Inhibitors
2.3 Selective N-Arylation of Nucleobases
2.4 Additional NH-Containing Substrates
3 C-O Cross-Coupling
3.1 Intermolecular C-O Cross-Coupling
3.2 Intramolecular C-O Cross-Coupling
4 Substrate Selectivity and Reactivity
5 Applications in Solid-Phase Synthesis
6 C-N and C-O Cross-Coupling with Boronic
Acid Derivatives
6.1 Boroxines, Boronic Esters, and Trifluoroborate Salts
6.2 Alkenylboronic Acids and Alkynylboronic Acids
6.3 Alkylboronic Acids
7 C-S and C-Se/C-Te Cross-Coupling
8 C-Cl, C-Br, and C-I Cross-Coupling
9 C-C and C-H Cross-Coupling
10 Mechanistic Considerations
10.1 Empirical Observations
10.2 General Mechanistic Observations
10.3 Mechanistic Study of the Catalytic Reaction
11 Other Transition Metals
12 Other Organometalloids
13 Conclusion
Key words
Chan-Lam coupling - copper-promoted - carbon-heteroatom cross-coupling - boronic
acids - N-arylation
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