| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5268932 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
A series of 3-diethoxyphosphorylquinolin-4-ones and 3-diethoxyphosphoryl-1,8-naphthyridin-4-ones containing various substituents at N-1 and C-7 was synthesized in a four-step reaction sequence starting from readily available ethyl 2-chlorobenzoates or ethyl 2-chloronicotinates and diethyl methylphosphonate. Selected quinolinone and naphthyridinone products were transformed into free mono and diacids.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jacek KÄdzia, Jakub Modranka, Tomasz Janecki,