Journal
CHEMISTRY LETTERS
Volume 42, Issue 6, Pages 583-585Publisher
CHEMICAL SOC JAPAN
DOI: 10.1246/cl.130116
Keywords
-
Categories
Funding
- MEXT, Japan
- Grants-in-Aid for Scientific Research [23710266, 24651257] Funding Source: KAKEN
Ask authors/readers for more resources
Arynes, generated in situ from o-(trimethylsilyl)aryl triflates by treatment with a fluoride, have been shown to react efficiently with various alkoxyphosphines via a mechanism similar to the Michaelis-Arbuzov reaction. Diverse aromatic oxophosphorus compounds, including derivatives with an ortho-ester function, have become easily available from a common aryne precursor by this method.
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