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Reactivity of cyanothioformamides and 3-(4-bromophenyl)-5-imino-4-oxazolidinethione toward ortho-substituted nucleophiles

✍ 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

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✦ Synopsis


Abstract

The substituted benzoazoles 4 and 5a,b were obtained by the reaction of cyanothioformamides 1d and 1b or 1c with o‐substituted aromatic amines 2b and 2c, respectively. Fused pyrimidinones 10, 12, and 14 were synthesized by the reaction of oxazolidinethione (9) with 2‐amino 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 13:611–616, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10042


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