2001
DOI: 10.1002/chin.200134166
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ChemInform Abstract: Synthesis of Oxygen‐Containing Heterocyclic ortho‐Dinitriles Based on 4‐Bromo‐5‐nitrophthalonitrile.

Abstract: ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

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“…Despite the progress made recently in this field, alternative methods of synthesizing these compounds continue to be developed. First of all, it should be noted that S N Ar-reactions occurring with the participation of 4-nitro-and 4-bromo-5-nitrophthalonitrile under homo-and hetero-conditions allow the study of the synthesis of a large number of diverse aromatic and heterocyclic compounds, [17][18][19][20][21][22][23] and related compounds that are condensed with the phthalonitrile fragment (Scheme1). In addition, we have developed methods for the synthesis of 3-substituted 2-amino-1-hydroxy-1H-indole-5,6-dicarbonitriles (2), [24] and 2-aryl-1-Hydroxy-1H-indole-5,6-dicarbonitriles (3), [25] based on 4-bromo-5-nitrophthalonitrile (1) (Scheme 2).…”
Section: Resultsmentioning
confidence: 99%
“…Despite the progress made recently in this field, alternative methods of synthesizing these compounds continue to be developed. First of all, it should be noted that S N Ar-reactions occurring with the participation of 4-nitro-and 4-bromo-5-nitrophthalonitrile under homo-and hetero-conditions allow the study of the synthesis of a large number of diverse aromatic and heterocyclic compounds, [17][18][19][20][21][22][23] and related compounds that are condensed with the phthalonitrile fragment (Scheme1). In addition, we have developed methods for the synthesis of 3-substituted 2-amino-1-hydroxy-1H-indole-5,6-dicarbonitriles (2), [24] and 2-aryl-1-Hydroxy-1H-indole-5,6-dicarbonitriles (3), [25] based on 4-bromo-5-nitrophthalonitrile (1) (Scheme 2).…”
Section: Resultsmentioning
confidence: 99%