2014
DOI: 10.1002/chin.201407199
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: An Efficient Synthetic Protocol for Quinoxalinones, Benzoxazinones, and Benzothiazinones from 2‐Oxo‐2‐aryl‐acetyl Bromide Precursors.

Abstract: Bromide Precursors. -Reaction of 2-oxo-2-arylacetyl bromides (II), obtained by SeO2 oxidation of α-bromoketones, with phenylenediamines, o-aminophenol, and o-aminothiophenol provides a facile and efficient access to quinoxalinones, benzoxazinones and benzothiazinones, respectively. -(NAGARAJ, M.; SATHIYAMOORTHY, S.; BOOMINATHAN, M.; MUTHUSUBRAMANIAN*, S.; BHUVANESH, N.; J. Heterocycl. Chem. 50 (2013) 5, 1146-1151, http://dx.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
0
0

Publication Types

Select...

Relationship

0
0

Authors

Journals

citations
Cited by 0 publications
references
References 1 publication
0
0
0
Order By: Relevance

No citations

Set email alert for when this publication receives citations?