Pyridine-Mediated B–B Bond Activation of (RO)₂B–B(OR)₂ for Generating Borylpyridine Anions and Pyridine-Stabilized Boryl Radicals as Useful Boryl Reagents in Organic Synthesis

Abstract

Significant developments have been achieved in recent years toward the utilization of (RO)₂B–B(OR)₂ for exploring transition-metal-free organic transformations in organic synthesis. Among the various combinations of Lewis bases with diborons developed so far, pyridine derivatives are simple, commercially available, and cheap compounds to expand the synthetic utility of diborons by generating borylpyridine anions and pyridine-stabilized boryl radicals via B–B bond cleavage. These borylpyridine species mediate a series of transformations in both a catalytic and stoichiometric manner for C–X activation (X = halogen, CO₂H, NR₂) and concomitant C-borylation, hydroboryl­ation, C–C bond formation, and reduction reactions.

1 Introduction

2 Reaction Pathway for B–B Bond Cleavage of Diborons with Electron-Deficient Pyridines

3 Pyridine-Mediated B–B Bond Activation of (RO)₂B–B(OR)₂ for Application in Organic Synthesis

3.1 Dehalogenative C-Borylation

3.2 Desulfonative C-Borylation

3.3 Decarboxylative C-Borylation

3.4 Deaminative C-Borylation

3.5 Hydroborylation

3.6 C–C Bond Formation

3.7 Pyridine Functionalization

3.8 Deoxygenation and N-Borylation Reactions

4 Conclusions

Key words

diboron - pyridine - B–B bond cleavage - borylation - single-electron transfer - radical reaction

Publikationsverlauf

Eingereicht: 03. März 2021

Angenommen nach Revision: 20. April 2021

Accepted Manuscript online:
20. April 2021

Artikel online veröffentlicht:
25. Mai 2021

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