4.8 Review

Organoboron compounds as versatile reagents in the transition metal-catalyzed C-S, C-Se and C-Te bond formation

Journal

COORDINATION CHEMISTRY REVIEWS
Volume 442, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.ccr.2021.214012

Keywords

Organoboron; Cross-coupling; Catalysis; Copper; Silver; Organochalcogen

Funding

  1. CNPq
  2. FAPERGS [PRONEM 16/2551-0000240-1]
  3. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior-Brasil (CAPES) [001]

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Organochalcogen compounds have significant synthetic and biological applications. The coupling reaction between boronic acids, borate anions or boronic esters with different sources of chalcogen mediated by transition metals is a powerful tool for the formation of functionalized diorganyl chalcogenides. This strategy allows for the preparation of selenides, sulfides, and tellurides with high complexity and molecular diversity in good to excellent yields.
Organochalcogen compounds present synthetic and biological applications of extreme relevance. The coupling reaction between boronic acids, borate anions or boronic esters with different sources of chalcogen (S, Se and Te), mediated by transition metals, is a powerful tool for the formation of functionalized diorganyl chalcogenides. By this strategy, selenides, sulfides, and tellurides with high complexity and molecular diversity can be prepared in good to excellent yields. This review covers the use of organo-boron compounds as a versatile reagent for the formation of Carbon-Chalcogen bonds using different metallic catalysts (Cu, Ag, Pd, Fe, In, Rh, Ni). (C) 2021 Elsevier B.V. All rights reserved.

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