4.8 Article

Oxyboration with and without a Catalyst: Borylated Isoxazoles via B-O σ-Bond Addition

Journal

ORGANIC LETTERS
Volume 18, Issue 3, Pages 480-483

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b03530

Keywords

-

Funding

  1. NIH [1R01GM098512-01]
  2. University of California, Irvine

Ask authors/readers for more resources

Herein we report an oxyboration reaction with activated substrates that employs B-O sigma bond additions to C-C pi bonds to form borylated isoxazoles, which are potential building blocks for drug discovery. Although this reaction can be effectively catalyzed by gold, it is the first example of uncatalyzed oxyboration of C-C pi bonds by B-O sigma bonds-and only the second example that is catalyzed. This oxyboration reaction is tolerant of groups incompatible with alternative lithiation/borylation and palladium-catalyzed C-H activation/borylation technologies for the synthesis of borylated isoxazoles.

Authors

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

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available