Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 142, Issue 28, Pages 11988-11992Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c04159
Keywords
-
Categories
Funding
- University of Delaware (UD)
- University of San Diego (USD)
- Camille and Henry Dreyfus Foundation
- National Science Foundation [CHE-1800011, CHE1764307]
- NSF [CHE-0421224, CHE-1048367, CHE-0840401]
- NIH [P20GM104316, P30GM110758, S10RR02692, S10OD016267]
Ask authors/readers for more resources
Phosphonate-directed ortho C-H borylation of aromatic phosphonates is reported. Using simple starting materials and commercially accessible catalysts, this method provides steady access to o-phosphonate arylboronic esters bearing pendant functionality and flexible substitution patterns. These products serve as flexible precursors for a variety of highly substituted phosphoarenes, and in situ downstream functionalization of the products is described.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available
Share Paper
