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Transition Metal-Free ipso-Functionalization of Arylboronic Acids and Derivatives

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 356, Issue 11-12, Pages 2395-2410

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201400305

Keywords

amination; arylboronic acids; halogenation; hydroxylation; transition metal-free conditions

Funding

  1. Soochow University
  2. The Project of Scientific and Technologic Infrastructure of Suzhou [SZS201207]
  3. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  4. Robert A. Welch Foundation [GL625910]
  5. NIH [GM31278]

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Arylboronic acids and their derivatives have been widely exploited as important synthetic precursors in organic synthesis, materials science, and pharmaceutical development. In addition to numerous applications in transition metal-mediated cross-coupling reactions, transition metal-free transformations involving arylboronic acids and derivatives have recently received a surge of attention for converting the C-B bond to C-C, C-N, C-O, and many other C-X bonds. Consequently, a wide range of useful compounds, e. g., phenols, anilines, nitroarenes, and haloarenes, has been readily synthesized. Amongst these efforts, many versatile reagents have been developed and a lot of practical approaches demonstrated. The research in this promising field is summarized in the current review and organized on the basis of the type of bonds being formed.

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