Easy access to polyhalogenated biaryls: regioselective (di)halogenation of hypervalent bromines and chlorines

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Easy access to polyhalogenated biaryls: regioselective (di)halogenation of hypervalent bromines and chlorines

Abstract: Polyhalogenated biaryls are unique motifs offering untapped potential as versatile building blocks for the expedient synthesis of complex biaryl compounds.

Cited by 3 publications

References 73 publications

[3 + 2] cycloaddition between cyclic diaryl λ³-bromanes and nitrones towards the formation of dihydrobenzisoxazoles and an evaluation of regioisomeric bioactivity

[3 + 2] cycloaddition between cyclic diaryl λ³-bromanes and nitrones towards the formation of dihydrobenzisoxazoles and an evaluation of regioisomeric bioactivity

Metal-free site-selective functionalization with cyclic diaryl λ³-chloranes: suppression of benzyne formation for ligand-coupling reactions

Regioselective Polyhalogenation of Biaryls via Hypervalent Halide

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Easy access to polyhalogenated biaryls: regioselective (di)halogenation of hypervalent bromines and chlorines

Abstract: Polyhalogenated biaryls are unique motifs offering untapped potential as versatile building blocks for the expedient synthesis of complex biaryl compounds.

Cited by 3 publications

References 73 publications

[3 + 2] cycloaddition between cyclic diaryl λ3-bromanes and nitrones towards the formation of dihydrobenzisoxazoles and an evaluation of regioisomeric bioactivity

[3 + 2] cycloaddition between cyclic diaryl λ3-bromanes and nitrones towards the formation of dihydrobenzisoxazoles and an evaluation of regioisomeric bioactivity

Metal-free site-selective functionalization with cyclic diaryl λ3-chloranes: suppression of benzyne formation for ligand-coupling reactions

Regioselective Polyhalogenation of Biaryls via Hypervalent Halide

Contact Info

Product

Resources

About

[3 + 2] cycloaddition between cyclic diaryl λ³-bromanes and nitrones towards the formation of dihydrobenzisoxazoles and an evaluation of regioisomeric bioactivity

[3 + 2] cycloaddition between cyclic diaryl λ³-bromanes and nitrones towards the formation of dihydrobenzisoxazoles and an evaluation of regioisomeric bioactivity

Metal-free site-selective functionalization with cyclic diaryl λ³-chloranes: suppression of benzyne formation for ligand-coupling reactions