Reactivity of Functionally Substituted Azoles Towards Electrophiles. Novel Synthesis of Thienylazoles and Phenylazoles
β Scribed by Abdel-Megid, Mohamed
- Book ID
- 119963579
- Publisher
- Taylor and Francis Group
- Year
- 2003
- Tongue
- English
- Weight
- 169 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0039-7911
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ΟβAzolylacetophenones **1** and **2** react with dimethylformamide dimethylacetal to yield enaminones **7,8** that were converted into azolylazoles __via__ reaction with hydrazine and with hydroxylamine. Compounds **1,2** also coupled with aromatic diazonium salts to yield arylhydrazone
## Abstract The reactivity of benzotriazolylacetone toward a variety of carbon and nitrogen electrophiles is reported. Several novel azolylbenzotriazoles as well as benzotriazolylβcinnolines have been synthesized. Β© 2002 Wiley Periodicals, Inc. Heteroatom Chem 13:141β145, 2002; Published online in