4.4 Article

Organoboron chemistry comes to light: Recent advances in photoinduced synthetic approaches to organoboron compounds

Journal

TETRAHEDRON
Volume 75, Issue 5, Pages 584-602

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2018.12.040

Keywords

Borylation; Carboboration; Diboron reagents; Photochemistry; Organoboron compounds; Rearrangements; Ring contraction

Funding

  1. Welch Foundation [AX-1788]
  2. NSF [CHE-1455061]
  3. NIGMS [SC3GM105579]
  4. Max and Minnie Tomerlin Voelcker Fund
  5. Brown Foundation

Ask authors/readers for more resources

Photoinduced synthetic approaches to organoboron compounds have attracted significant attention in the recent years. Photochemical activation of organic molecules enables generation of reactive intermediates from a variety of precursors, resulting in borylation methods with improved and broader substrate scopes. The review summarizes recent developments in the area of photoinduced reactions of organoboron compounds with an emphasis on borylation of haloarenes, amine derivatives, and redox-active esters of carboxylic acids, as well as photoinduced rearrangements of organoboron compounds and photoinduced synthesis of organoboron compounds from alkenes and alkynes. (C) 2018 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available