Oxone-mediated oxidative carbon-heteroatom bond cleavage: synthesis of benzoxazinones from benzoxazoles with α-oxocarboxylic acids
H Wang, H Yang, Y Li, XH Duan
Index: RSC Advances, , vol. 4, # 17 p. 8720 - 8722
Full Text: HTML
Citation Number: 11
Abstract
... RSC Adv., 2014, 4, 8720-8722. ... 8, —, 5% DMSO/Diglyme, Nr c. 9, (NH 4 ) 2 S 2 O 8 (1.0), 5% DMSO/Diglyme, 26. ... image file: c3ra47660j-u2.tif. Various substituted α-oxocarboxylic acids were then tested for this oxidative cleavage/coupling reaction under the optimized conditions. ...
Related Articles:
A convenient synthesis of 3, 4-dihydro-1, 4-benzoxazin-2-ones
[Tetrahedron, , vol. 64, # 24 p. 5756 - 5761]
[Chemical and pharmaceutical bulletin, , vol. 28, # 11 p. 3437 - 3439]
Direct conversion of anilines into aminophenols
[Tetrahedron Letters, , vol. 25, # 14 p. 1479 - 1482]
[Croatica Chemica Acta, , vol. 85, # 3 p. 277 - 282]
[Zoran, Ami; Khodzhaev, Oleg; Sasson, Yoel Journal of the Chemical Society, Chemical Communications, 1994 , # 19 p. 2239 - 2240]