Please use this identifier to cite or link to this item:
|Title:||Solid-phase combinatorial synthesis of 4-hydroxyquinolin-2(1H)-ones||Authors:||Sim, M.M.
|Issue Date:||27-Aug-1998||Citation:||Sim, M.M., Lee, C.L., Ganesan, A. (1998-08-27). Solid-phase combinatorial synthesis of 4-hydroxyquinolin-2(1H)-ones. Tetrahedron Letters 39 (35) : 6399-6402. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4039(98)01320-3||Abstract:||Cyanoacetic acid was loaded on Wang resin and C-acylated using acid anhydrides and triethylamine as base. Resin cleavage with concomitant decarboxylation produces β-keto nitriles. In the case of isatoic anhydrides, the resin-bound acylated intermediates undergo cyclative cleavage upon heating, leading to 4hydroxyquinolin-2(1H)-ones.||Source Title:||Tetrahedron Letters||URI:||http://scholarbank.nus.edu.sg/handle/10635/112075||ISSN:||00404039||DOI:||10.1016/S0040-4039(98)01320-3|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Oct 22, 2020
WEB OF SCIENCETM
checked on Oct 14, 2020
checked on Oct 23, 2020
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.