Reactivity of cyanothioformamides and 3-(4-bromophenyl)-5-imino-4-oxazolidinethione toward ortho-substituted nucleophiles
β Scribed by Mohamed S. A. El-Gaby; Yousry A. Ammar; Ahmed M. Sh. El-Sharief; Medhat A. Zahran; Ahmed A. Khames
- Book ID
- 102230799
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 104 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.10042
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β¦ Synopsis
Abstract
The substituted benzoazoles 4 and 5a,b were obtained by the reaction of cyanothioformamides 1d and 1b or 1c with oβsubstituted aromatic amines 2b and 2c, respectively. Fused pyrimidinones 10, 12, and 14 were synthesized by the reaction of oxazolidinethione (9) with 2βamino aromatic and heteroaromatic carboxylic acids. The structures of the synthesized compounds were established based on elemental analysis and spectral data studies. Β© 2002 Wiley Periodicals, Inc. Heteroatom Chem 13:611β616, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10042
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